Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: MMP9 (Hsa)
(GRCh38)20:46012536G>C
(Homo sapiens)Allele/Variant
Source: rs762864452
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012536G>C
(GRCh38)20:46014174C>G
(Homo sapiens)Allele/Variant
Source: rs527990566
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46014174C>G
(GRCh38)20:46014210G>C
(Homo sapiens)Allele/Variant
Source: rs1319203113
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46014210G>C
(GRCh38)20:46013338C>T
(Homo sapiens)Allele/Variant
Source: rs148151404
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46013338C>T
(GRCh38)20:46008996C>T
(Homo sapiens)Allele/Variant
Source: rs144023823
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46008996C>T
(GRCh38)20:46010115G>A
(Homo sapiens)Allele/Variant
Source: rs748177749
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010115G>A
(GRCh38)20:46011253C>A
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.46011253C>A
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46011253C>A
(GRCh38)20:46011275A>G
(Homo sapiens)Allele/Variant
Source: rs144229833
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46011275A>G
(GRCh38)20:46011330C>T
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.46011330C>T
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46011330C>T
(GRCh38)20:46011566C>T
(Homo sapiens)Allele/Variant
Source: rs2084278728
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46011566C>T
(GRCh38)20:46010110C>T
(Homo sapiens)Allele/Variant
Source: rs199711234
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010110C>T
(GRCh38)20:46010332A>C
(Homo sapiens)Allele/Variant
Source: rs79845319
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010332A>C
(GRCh38)20:46012229G>A
(Homo sapiens)Allele/Variant
Source: rs1262533864
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012229G>A
(GRCh38)20:46012448C>T
(Homo sapiens)Allele/Variant
Source: rs200590350
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012448C>T
(GRCh38)20:46012460T>A
(Homo sapiens)Allele/Variant
Source: rs201417784
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012460T>A
(GRCh38)20:46012502C>T
(Homo sapiens)Allele/Variant
Source: rs771043300
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012502C>T
(GRCh38)20:46012504C>T
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.46012504C>T
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012504C>T
(GRCh38)20:46012538C>A
(Homo sapiens)Allele/Variant
Source: rs146895638
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012538C>A
(GRCh38)20:46012540C>T
(Homo sapiens)Allele/Variant
Source: rs754588801
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012540C>T
(GRCh38)20:46011678G>C
(Homo sapiens)Allele/Variant
Source: rs749575889
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46011678G>C
(GRCh38)20:46009861C>T
(Homo sapiens)Allele/Variant
Source: rs200040822
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46009861C>T
(GRCh38)20:46010634G>A
(Homo sapiens)Allele/Variant
Source: rs773948750
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010634G>A
(GRCh38)20:46009006C>T
(Homo sapiens)Allele/Variant
Source: rs201841087
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46009006C>T
(GRCh38)20:46009039A>G
(Homo sapiens)Allele/Variant
Source: rs41427445
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46009039A>G
(GRCh38)20:46008985C>T
(Homo sapiens)Allele/Variant
Source: rs1805088
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46008985C>T
(GRCh38)20:46009013G>T
(Homo sapiens)Allele/Variant
Source: rs753482129
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46009013G>T
(GRCh38)20:46010053C>T
(Homo sapiens)Allele/Variant
Source: rs200316960
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010053C>T
(GRCh38)20:46010071A>G
(Homo sapiens)Allele/Variant
Source: rs202158739
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010071A>G
(GRCh38)20:46010575C>T
(Homo sapiens)Allele/Variant
Source: rs143024943
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010575C>T
(GRCh38)20:46010569C>A
(Homo sapiens)Allele/Variant
Source: rs753889026
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010569C>A
(GRCh38)20:46010093C>A
(Homo sapiens)Allele/Variant
Source: rs200290957
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010093C>A
(GRCh38)20:46010105C>G
(Homo sapiens)Allele/Variant
Source: rs1568846477
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010105C>G
(GRCh38)20:46010649G>A
(Homo sapiens)Allele/Variant
Source: rs930335677
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46010649G>A
(GRCh38)20:46009019C>T
(Homo sapiens)Allele/Variant
Source: rs200436945
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46009019C>T
(GRCh38)20:46011735T>G
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.46011735T>G
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46011735T>G
(GRCh38)20:46011737C>T
(Homo sapiens)Allele/Variant
Source: rs1302101551
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46011737C>T
(GRCh38)20:46013781C>T
(Homo sapiens)Allele/Variant
Source: rs2084301336
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46013781C>T
(GRCh38)20:46014237G>C
(Homo sapiens)Allele/Variant
Source: rs773448293
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46014237G>C
(GRCh38)20:46014261C>T
(Homo sapiens)Allele/Variant
Source: rs1233986311
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46014261C>T
(GRCh38)20:46014264C>A
(Homo sapiens)Allele/Variant
Source: rs201280938
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46014264C>A
(GRCh38)20:46012181G>T
(Homo sapiens)Allele/Variant
Source: rs1408103367
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012181G>T
(GRCh38)20:46012205A>G
(Homo sapiens)Allele/Variant
Source: rs200855672
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012205A>G
(GRCh38)20:46012306G>C
(Homo sapiens)Allele/Variant
Source: rs200232624
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012306G>C
(GRCh38)20:46012312A>C
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.46012312A>C
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012312A>C
(GRCh38)20:46012414C>G
(Homo sapiens)Allele/Variant
Source: rs374362256
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46012414C>G
(GRCh38)20:46014352C>A
(Homo sapiens)Allele/Variant
Source: rs200290639
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46014352C>A
(GRCh38)20:46014381A>C
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.46014381A>C
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46014381A>C
(GRCh38)20:46014446G>A
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.46014446G>A
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46014446G>A
(GRCh38)20:46016352A>G
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.46016352A>G
Genes: SLC12A5-AS1 (Hsa), MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46016352A>G
(GRCh38)20:46011729G>C
(Homo sapiens)Allele/Variant
Source: rs199569524
Genes: MMP9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:46011729G>C