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Select item 23844721.

rs2384472 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:54555722 (GRCh38)
10:56315482 (GRCh37)
Canonical SPDI:: NC_000010.11:54555721:G:A,NC_000010.11:54555721:G:T
Gene:: PCDH15 (Varview), LOC105378311 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.13929/1947 (ALFA)
A=0.159554/2669 (TOMMO)
A=0.179781/329 (Korea1K)
A=0.190281/556 (KOREAN)
A=0.215022/1077 (1000Genomes)
A=0.217441/955 (Estonian)
A=0.256258/31797 (GnomAD)
A=0.258484/68418 (TOPMED)
A=0.289579/289 (GoNL)
A=0.291532/1081 (TWINSUK)
A=0.300467/1158 (ALSPAC)
A=0.323427/185 (NorthernSweden)
A=0.35/14 (GENOME_DK)
A=0.37037/80 (Qatari)
G=0.42/105 (SGDP_PRJ)
G=0.428571/12 (Siberian)
HGVS:: NC_000010.11:g.54555722G>A, NC_000010.11:g.54555722G>T, NC_000010.10:g.56315482G>A, NC_000010.10:g.56315482G>T, NG_009191.3:g.1078461C>T, NG_009191.3:g.1078461C>A

dbSNP