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Select item 26651.

rs2665 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:71549302 (GRCh38)
11:71260348 (GRCh37)
Canonical SPDI:: NC_000011.10:71549301:T:A,NC_000011.10:71549301:T:C
Gene:: KRTAP5-9 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.085155/1332 (ALFA)
A=0.075/3 (GENOME_DK)
A=0.084112/18 (Vietnamese)
A=0.099637/384 (ALSPAC)
A=0.105987/393 (TWINSUK)
A=0.11/66 (NorthernSweden)
A=0.113618/8799 (TOMMO)
A=0.116232/116 (GoNL)
A=0.129021/377 (KOREAN)
A=0.131086/70 (MGP)
A=0.138513/1002 (Korea4K)
A=0.145197/266 (Korea1K)
A=0.166071/744 (Estonian)
A=0.181818/60 (HapMap)
A=0.182109/912 (1000Genomes)
A=0.184104/1179 (1000Genomes_30X)
A=0.184397/48808 (TOPMED)
A=0.268519/58 (Qatari)
T=0.458333/11 (Siberian)
T=0.459016/56 (SGDP_PRJ)
HGVS:: NC_000011.10:g.71549302T>A, NC_000011.10:g.71549302T>C, NC_000011.9:g.71260348T>A, NC_000011.9:g.71260348T>C, NG_123406.1:g.564T>A, NG_123406.1:g.564T>C, NM_005553.4:c.*135T>A, NM_005553.4:c.*135T>C, NM_005553.3:c.*135T>A, NM_005553.3:c.*135T>C

Supplemental Content

dbSNP