Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SNCA (Hsa) Molecular Consequence: missense variant
(GRCh38)4:89822180C>T
(Homo sapiens)Allele/Variant
Source: rs10005233
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822180C>T
(GRCh38)4:89822309T>C
(Homo sapiens)Allele/Variant
Source: rs568436589
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822309T>C
(GRCh38)4:89835536G>A
(Homo sapiens)Allele/Variant
Source: rs35135226
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835536G>A
(GRCh38)4:89835563C>T
(Homo sapiens)Allele/Variant
Source: rs768334864
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835563C>T
(GRCh38)4:89835569T>C
(Homo sapiens)Allele/Variant
Source: rs766497794
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835569T>C
(GRCh38)4:89726714T>C
(Homo sapiens)Allele/Variant
Source: rs6842093
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726714T>C
(GRCh38)4:89835566T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.89835566T>C
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835566T>C
(GRCh38)4:89822369C>T
(Homo sapiens)Allele/Variant
Source: rs1737231816
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822369C>T
(GRCh38)4:89725998A>C
(Homo sapiens)Allele/Variant
Source: rs886059725
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89725998A>C
(GRCh38)4:89724591A>G
(Homo sapiens)Allele/Variant
Source: rs553070344
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89724591A>G
(GRCh38)4:89746090C>G
(Homo sapiens)Allele/Variant
Source: rs207464865
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89746090C>G
(GRCh38)4:89729187C>G
(Homo sapiens)Allele/Variant
Source: rs370797923
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729187C>G
(GRCh38)4:89729209A>G
(Homo sapiens)Allele/Variant
Source: rs367556974
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729209A>G
(GRCh38)4:89828150C>A
(Homo sapiens)Allele/Variant
Source: rs148108612
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828150C>A
(GRCh38)4:89835659T>C
(Homo sapiens)Allele/Variant
Source: rs370989462
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835659T>C
(GRCh38)4:89822239G>A
(Homo sapiens)Allele/Variant
Source: rs2110460139
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822239G>A
(GRCh38)4:89822704C>G
(Homo sapiens)Allele/Variant
Source: rs7356228
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822704C>G
(GRCh38)4:89828284T>G
(Homo sapiens)Allele/Variant
Source: rs34183114
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828284T>G
(GRCh38)4:89835475C>T
(Homo sapiens)Allele/Variant
Source: rs35009676
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835475C>T
(GRCh38)4:89822254A>G
(Homo sapiens)Allele/Variant
Source: rs138969470
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822254A>G
(GRCh38)4:89822303C>T
(Homo sapiens)Allele/Variant
Source: rs1737224483
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822303C>T
(GRCh38)4:89828186T>G
(Homo sapiens)Allele/Variant
Source: rs2110488615
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828186T>G
(GRCh38)4:89828320T>A
(Homo sapiens)Allele/Variant
Source: rs554831708
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828320T>A
(GRCh38)4:89836976C>T
(Homo sapiens)Allele/Variant
Source: rs886059729
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89836976C>T
(GRCh38)4:89827981A>G
(Homo sapiens)Allele/Variant
Source: rs1442149
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89827981A>G
(GRCh38)4:89828136A>C
(Homo sapiens)Allele/Variant
Source: rs1578405610
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828136A>C
(GRCh38)4:89828137G>T
(Homo sapiens)Allele/Variant
Source: rs2110488377
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828137G>T
(GRCh38)4:89726643G>A
(Homo sapiens)Allele/Variant
Source: rs76642636
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726643G>A
(GRCh38)4:89822336C>T
(Homo sapiens)Allele/Variant
Source: rs144758871
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822336C>T
(GRCh38)4:89822496A>T
(Homo sapiens)Allele/Variant
Source: rs11944927
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822496A>T
(GRCh38)4:89822327T>A
(Homo sapiens)Allele/Variant
Source: rs149401968
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822327T>A
(GRCh38)4:89835560A>G
(Homo sapiens)Allele/Variant
Source: rs1407062582
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835560A>G
(GRCh38)4:89729183T>G
(Homo sapiens)Allele/Variant
Source: rs546366532
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729183T>G
(GRCh38)4:89822306C>T
(Homo sapiens)Allele/Variant
Source: rs775179895
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822306C>T
(GRCh38)4:89822404A>T
(Homo sapiens)Allele/Variant
Source: rs762146888
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822404A>T
(GRCh38)4:89836961C>T
(Homo sapiens)Allele/Variant
Source: rs1560562993
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89836961C>T
(GRCh38)4:89726676T>C
(Homo sapiens)Allele/Variant
Source: rs371014092
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726676T>C
(GRCh38)4:89827937T>C
(Homo sapiens)Allele/Variant
Source: rs36014224
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89827937T>C
(GRCh38)4:89835382C>T
(Homo sapiens)Allele/Variant
Source: rs141771108
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835382C>T
(GRCh38)4:89835399C>G
(Homo sapiens)Allele/Variant
Source: rs7681440
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835399C>G
(GRCh38)4:89724926C>T
(Homo sapiens)Allele/Variant
Source: rs886059714
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89724926C>T
(GRCh38)4:89725110A>G
(Homo sapiens)Allele/Variant
Source: rs1724761878
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89725110A>G
(GRCh38)4:89725339A>G
(Homo sapiens)Allele/Variant
Source: rs527798413
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89725339A>G
(GRCh38)4:89725341C>A
(Homo sapiens)Allele/Variant
Source: rs377356638
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89725341C>A
(GRCh38)4:89724298G>A
(Homo sapiens)Allele/Variant
Source: rs886059712
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89724298G>A
(GRCh38)4:89724401G>T
(Homo sapiens)Allele/Variant
Source: rs551886776
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89724401G>T
(GRCh38)4:89725705T>C
(Homo sapiens)Allele/Variant
Source: rs925720552
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89725705T>C
(GRCh38)4:89725768A>T
(Homo sapiens)Allele/Variant
Source: rs577490090
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89725768A>T
(GRCh38)4:89726035G>T
(Homo sapiens)Allele/Variant
Source: rs35101723
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726035G>T
(GRCh38)4:89726512G>A
(Homo sapiens)Allele/Variant
Source: rs144511886
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726512G>A