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rs16936752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs16936752(G;G)
Make rs16936752(G;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position93301408
GeneWNK2
is asnp
is mentioned by
dbSNPrs16936752
ebirs16936752
HLIrs16936752
Exacrs16936752
Varsomers16936752
Maprs16936752
PheGenIrs16936752
hapmaprs16936752
1000 genomesrs16936752
hgdprs16936752
ensemblrs16936752
gopubmedrs16936752
geneviewrs16936752
scholarrs16936752
googlers16936752
pharmgkbrs16936752
gwascentralrs16936752
openSNPrs16936752
23andMers16936752
23andMe allrs16936752
SNP Nexus

SNPshotrs16936752
SNPdbers16936752
MSV3drs16936752
GWAS Ctlgrs16936752
GMAF0.08907
Max Magnitude0
? (G;G) (G;T) (T;T) 28

[PMID 20198315] Association of genetic variants with hemorrhagic stroke in Japanese individuals