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rs4977950

From SNPedia

Orientationplus
Stabilizedplus
Make rs4977950(C;C)
Make rs4977950(C;G)
Make rs4977950(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position24732484
is asnp
is mentioned by
dbSNPrs4977950
ebirs4977950
HLIrs4977950
Exacrs4977950
Varsomers4977950
Maprs4977950
PheGenIrs4977950
hapmaprs4977950
1000 genomesrs4977950
hgdprs4977950
ensemblrs4977950
gopubmedrs4977950
geneviewrs4977950
scholarrs4977950
googlers4977950
pharmgkbrs4977950
gwascentralrs4977950
openSNPrs4977950
23andMers4977950
23andMe allrs4977950
SNP Nexus

SNPshotrs4977950
SNPdbers4977950
MSV3drs4977950
GWAS Ctlgrs4977950
GMAF0.3563
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 23151749] Lack of association between STK39 and hypertension in the Chinese population [PMID 19114657OA-icon.png] From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.


[PMID 20003416OA-icon.png] STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression.