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Select item 22917261.

rs2291726 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 17:48961892 (GRCh38)
17:47039254 (GRCh37)
Canonical SPDI:: NC_000017.11:48961891:T:A,NC_000017.11:48961891:T:C
Gene:: GIP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.461184/76028 (ALFA)
C=0.251899/199 (PRJEB37584)
C=0.252212/4227 (TOMMO)
C=0.258703/758 (KOREAN)
C=0.265284/486 (Korea1K)
T=0.3/129 (SGDP_PRJ)
T=0.321429/9 (Siberian)
C=0.330189/70 (Vietnamese)
C=0.367041/196 (MGP)
T=0.407407/88 (Qatari)
T=0.421164/796 (HapMap)
T=0.434191/114926 (TOPMED)
T=0.439313/61488 (GnomAD)
T=0.441599/2212 (1000Genomes)
C=0.45/18 (GENOME_DK)
C=0.45/270 (NorthernSweden)
C=0.450917/1672 (TWINSUK)
C=0.45491/454 (GoNL)
C=0.468345/1805 (ALSPAC)
C=0.474107/2124 (Estonian)
HGVS:: NC_000017.11:g.48961892T>A, NC_000017.11:g.48961892T>C, NC_000017.10:g.47039254T>A, NC_000017.10:g.47039254T>C