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rs5945919

From SNPedia

Orientationplus
Stabilizedplus
Make rs5945919(A;A)
Make rs5945919(A;G)
Make rs5945919(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position102963359
is asnp
is mentioned by
dbSNPrs5945919
ebirs5945919
HLIrs5945919
Exacrs5945919
Varsomers5945919
Maprs5945919
PheGenIrs5945919
hapmaprs5945919
1000 genomesrs5945919
hgdprs5945919
ensemblrs5945919
gopubmedrs5945919
geneviewrs5945919
scholarrs5945919
googlers5945919
pharmgkbrs5945919
gwascentralrs5945919
openSNPrs5945919
23andMers5945919
23andMe allrs5945919
SNP Nexus

SNPshotrs5945919
SNPdbers5945919
MSV3drs5945919
GWAS Ctlgrs5945919
GMAF0.1566
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24209690] An X-chromosomal association study identifies a susceptibility locus at Xq22.1 for hepatitis B virus-related hepatocellular carcinoma