Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: APP (Hsa)
(GRCh38)21:25955709T>G
(Homo sapiens)Allele/Variant
Source: rs1555902848
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25955709T>G
(GRCh38)21:25955751C>T
(Homo sapiens)Allele/Variant
Source: rs200587958
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25955751C>T
(GRCh38)21:25982445C>T
(Homo sapiens)Allele/Variant
Source: rs141331202
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25982445C>T
(GRCh38)21:26022152A>G
(Homo sapiens)Allele/Variant
Source: rs45451592
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26022152A>G
(GRCh38)21:26051088C>T
(Homo sapiens)Allele/Variant
Source: rs759517529
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26051088C>T
(GRCh38)21:26112083G>C
(Homo sapiens)Allele/Variant
Source: rs886056997
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26112083G>C
(GRCh38)21:25880757G>C
(Homo sapiens)Allele/Variant
Source: rs202081585
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25880757G>C
(GRCh38)21:25954442T>A
(Homo sapiens)Allele/Variant
Source: rs2829996
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25954442T>A
(GRCh38)21:25955621G>A
(Homo sapiens)Allele/Variant
Source: rs758516154
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25955621G>A
(GRCh38)21:25881664G>A
(Homo sapiens)Allele/Variant
Source: rs376555983
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25881664G>A
(GRCh38)21:25891800G>T
(Homo sapiens)Allele/Variant
Source: rs116650065
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25891800G>T
(GRCh38)21:25911754G>A
(Homo sapiens)Allele/Variant
Source: rs2146319673
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911754G>A
(GRCh38)21:25911837C>G
(Homo sapiens)Allele/Variant
Source: rs374799888
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911837C>G
(GRCh38)21:25911875G>A
(Homo sapiens)Allele/Variant
Source: rs754790092
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911875G>A
(GRCh38)21:25911928A>G
(Homo sapiens)Allele/Variant
Source: rs201794320
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911928A>G
(GRCh38)21:25982446G>A
(Homo sapiens)Allele/Variant
Source: rs780257087
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25982446G>A
(GRCh38)21:26021954C>T
(Homo sapiens)Allele/Variant
Source: rs2044360130
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26021954C>T
(GRCh38)21:26051041A>G
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.26051041A>G
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26051041A>G
(GRCh38)21:26051070A>G
(Homo sapiens)Allele/Variant
Source: rs145081708
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26051070A>G
(GRCh38)21:26089951C>T
(Homo sapiens)Allele/Variant
Source: rs2061787725
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26089951C>T
(GRCh38)21:25891793T>C
(Homo sapiens)Allele/Variant
Source: rs63750643
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25891793T>C
(GRCh38)21:25975725G>A
(Homo sapiens)Allele/Variant
Source: rs151039390
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25975725G>A
(GRCh38)21:25975052G>A
(Homo sapiens)Allele/Variant
Source: rs200083249
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25975052G>A
(GRCh38)21:25904928T>A
(Homo sapiens)Allele/Variant
Source: rs45467193
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25904928T>A
(GRCh38)21:26090080A>G
(Homo sapiens)Allele/Variant
Source: rs1172073288
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26090080A>G
(GRCh38)21:26170608A>C
(Homo sapiens)Allele/Variant
Source: rs1446208112
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26170608A>C
(GRCh38)21:25891786A>G
(Homo sapiens)Allele/Variant
Source: rs63750851
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25891786A>G
(GRCh38)21:25955684C>G
(Homo sapiens)Allele/Variant
Source: rs767201930
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25955684C>G
(GRCh38)21:25975112G>A
(Homo sapiens)Allele/Variant
Source: rs201377759
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25975112G>A
(GRCh38)21:25975148T>C
(Homo sapiens)Allele/Variant
Source: rs745834578
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25975148T>C
(GRCh38)21:26170819C>T
(Homo sapiens)Allele/Variant
Source: rs761755102
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26170819C>T
(GRCh38)21:25911861A>C
(Homo sapiens)Allele/Variant
Source: rs773379255
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911861A>C
(GRCh38)21:25911957G>C
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.25911957G>C
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911957G>C
(GRCh38)21:26051171T>C
(Homo sapiens)Allele/Variant
Source: rs1231783932
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26051171T>C
(GRCh38)21:25911966A>C
(Homo sapiens)Allele/Variant
Source: rs374277868
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911966A>C
(GRCh38)21:25955770T>A
(Homo sapiens)Allele/Variant
Source: rs1195877298
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25955770T>A
(GRCh38)21:25881883C>T
(Homo sapiens)Allele/Variant
Source: rs2829966
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25881883C>T
(GRCh38)21:25976147T>C
(Homo sapiens)Allele/Variant
Source: rs3737415
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25976147T>C
(GRCh38)21:26170790G>T
(Homo sapiens)Allele/Variant
Source: rs538664273
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26170790G>T
(GRCh38)21:25911880G>A
(Homo sapiens)Allele/Variant
Source: rs200150248
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911880G>A
(GRCh38)21:25997094T>C
(Homo sapiens)Allele/Variant
Source: rs8132220
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25997094T>C
(GRCh38)21:26090075G>A
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.26090075G>A
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26090075G>A
(GRCh38)21:25891809G>A
(Homo sapiens)Allele/Variant
Source: rs148888161
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25891809G>A
(GRCh38)21:25891820G>C
(Homo sapiens)Allele/Variant
Source: rs63750921
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25891820G>C
(GRCh38)21:25911841G>A
(Homo sapiens)Allele/Variant
Source: rs150151009
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911841G>A
(GRCh38)21:25891853C>T
(Homo sapiens)Allele/Variant
Source: rs63749810
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25891853C>T
(GRCh38)21:25891855T>C
(Homo sapiens)Allele/Variant
Source: rs63751039
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25891855T>C
(GRCh38)21:25897590C>T
(Homo sapiens)Allele/Variant
Source: rs762823452
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25897590C>T
(GRCh38)21:25975989T>G
(Homo sapiens)Allele/Variant
Source: rs2146575525
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25975989T>G
(GRCh38)21:25982404A>G
(Homo sapiens)Allele/Variant
Source: rs2042467013
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25982404A>G