Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: APP (Hsa) Molecular Consequence: non coding transcript variant
(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)21:25954442T>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)21:25997094T>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)21:25997374C>T
(Homo sapiens)Allele/Variant
Source: rs1057524107
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25997374C>T
(GRCh38)21:25975231G>T
(Homo sapiens)Allele/Variant
Source: rs1342453998
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)21:25975231G>T
(GRCh38)21:25975239A>C
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.25975239A>C
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25975239A>C
(GRCh38)21:26089931C>T
(Homo sapiens)Allele/Variant
Source: rs1295640613
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26089931C>T
(GRCh38)21:26053007C>T
(Homo sapiens)Allele/Variant
Source: rs6516719
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26053007C>T
(GRCh38)21:25891872G>A
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.25891872G>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)21:25891872G>A
(GRCh38)21:25975950T>C
(Homo sapiens)Allele/Variant
Source: rs945993637
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)21:25975950T>C
(GRCh38)21:25905294C>T
(Homo sapiens)Allele/Variant
Source: rs7279018
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25905294C>T
(GRCh38)21:25982704T>C
(Homo sapiens)Allele/Variant
Source: rs2070657
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25982704T>C
(GRCh38)21:25955861T>C
(Homo sapiens)Allele/Variant
Source: rs440666
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25955861T>C
(GRCh38)21:26000378G>C
(Homo sapiens)Allele/Variant
Source: rs28635874
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26000378G>C
(GRCh38)21:25997413G>T
(Homo sapiens)Allele/Variant
Source: rs1260561215
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25997413G>T
(GRCh38)21:26022049A>G
(Homo sapiens)Allele/Variant
Source: rs183084252
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)21:26022049A>G
(GRCh38)21:25976134A>G
(Homo sapiens)Allele/Variant
Source: rs3737414
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25976134A>G
(GRCh38)21:25997356G>A
(Homo sapiens)Allele/Variant
Source: rs532690231
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25997356G>A
(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)21:25881829A>C
(Homo sapiens)Allele/Variant
Source: rs41276546
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25881829A>C
(GRCh38)21:25975061G>A
(Homo sapiens)Allele/Variant
Source: rs201937048
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25975061G>A
(GRCh38)21:25911723G>T
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.25911723G>T
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911723G>T
(GRCh38)21:26053367A>C
(Homo sapiens)Allele/Variant
Source: rs761238827
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26053367A>C
(GRCh38)21:26140003T>C
(Homo sapiens)Allele/Variant
Source: rs9305281
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26140003T>C
(GRCh38)21:25881786G>A
(Homo sapiens)Allele/Variant
Source: rs1410825490
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25881786G>A
(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)21:26022052C>T
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.26022052C>T
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26022052C>T
(GRCh38)21:26089932G>A
(Homo sapiens)Allele/Variant
Source: rs113003524
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26089932G>A
(GRCh38)21:25997360G>A
(Homo sapiens)Allele/Variant
Source: rs749453173
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25997360G>A
(GRCh38)21:26111965C>T
(Homo sapiens)Allele/Variant
Source: rs199644062
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26111965C>T
(GRCh38)21:26000167T>C
(Homo sapiens)Allele/Variant
Source: rs1371336849
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26000167T>C
(GRCh38)21:25954545G>A
(Homo sapiens)Allele/Variant
Source: rs2829997
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25954545G>A
(GRCh38)21:26022051G>T
(Homo sapiens)Allele/Variant
Source: rs199587668
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26022051G>T
(GRCh38)21:26050815C>T
(Homo sapiens)Allele/Variant
Source: rs2830026
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:26050815C>T
(GRCh38)21:25954786G>A
(Homo sapiens)Allele/Variant
Source: rs417676
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25954786G>A
(GRCh38)21:25905006G>A
(Homo sapiens)Allele/Variant
Source: rs200910966
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25905006G>A
(GRCh38)21:25881987G>A
(Homo sapiens)Allele/Variant
Source: rs17001455
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25881987G>A
(GRCh38)21:25976073C>A
(Homo sapiens)Allele/Variant
Source: rs116447989
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25976073C>A
(GRCh38)21:25905237A>G
(Homo sapiens)Allele/Variant
Source: rs7278851
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25905237A>G
(GRCh38)21:25955548G>C
(Homo sapiens)Allele/Variant
Source: rs2251337
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25955548G>C
(GRCh38)21:25982328G>T
(Homo sapiens)Allele/Variant
Source: rs199585064
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25982328G>T
(GRCh38)21:25911732G>A
(Homo sapiens)Allele/Variant
Source: rs201352332
Genes: APP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:25911732G>A