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Select item 31681.

rs3168 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:41885326 (GRCh38)
21:43305435 (GRCh37)
Canonical SPDI:: NC_000021.9:41885325:C:T
Gene:: C2CD2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.151659/20302 (ALFA)
T=0.031835/17 (MGP)
C=0.092593/20 (Qatari)
C=0.101116/453 (Estonian)
C=0.115/69 (NorthernSweden)
C=0.132416/491 (TWINSUK)
C=0.135271/135 (GoNL)
C=0.136482/526 (ALSPAC)
C=0.145176/21657 (GnomAD_genomes)
C=0.149794/39649 (TOPMED)
C=0.15/6 (GENOME_DK)
C=0.164187/309 (HapMap)
C=0.175/91 (SGDP_PRJ)
C=0.179107/1147 (1000Genomes_30X)
C=0.182508/914 (1000Genomes)
C=0.198413/50 (GnomAD_exomes)
C=0.211538/11 (Siberian)
C=0.218907/16953 (TOMMO)
C=0.22107/405 (Korea1K)
C=0.22995/1663 (Korea4K)
C=0.235495/690 (KOREAN)
C=0.242991/52 (Vietnamese)
HGVS:: NC_000021.9:g.41885326C>T, NC_000021.8:g.43305435C>T, XM_005261109.5:c.*3798G>A, XM_005261109.3:c.*3798G>A, XM_005261109.2:c.*3798G>A, XM_005261109.1:c.*3798G>A, XM_011529523.3:c.*3798G>A, XM_011529523.1:c.*3798G>A, XM_011529522.3:c.*3798G>A, XM_011529522.2:c.*3798G>A, XM_011529522.1:c.*3798G>A, NM_199050.3:c.*3798G>A, NM_199050.2:c.*3798G>A, NM_015500.2:c.*3798G>A, NM_015500.1:c.*3798G>A, NM_198997.1:c.*3798G>A

dbSNP