Have questions? Visit https://www.reddit.com/r/SNPedia

rs6838973

From SNPedia

Orientationplus
Stabilizedplus
Make rs6838973(C;C)
Make rs6838973(C;T)
Make rs6838973(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position110844339
is asnp
is mentioned by
dbSNPrs6838973
ebirs6838973
HLIrs6838973
Exacrs6838973
Varsomers6838973
Maprs6838973
PheGenIrs6838973
hapmaprs6838973
1000 genomesrs6838973
hgdprs6838973
ensemblrs6838973
gopubmedrs6838973
geneviewrs6838973
scholarrs6838973
googlers6838973
pharmgkbrs6838973
gwascentralrs6838973
openSNPrs6838973
23andMers6838973
23andMe allrs6838973
SNP Nexus

SNPshotrs6838973
SNPdbers6838973
MSV3drs6838973
GWAS Ctlgrs6838973
GMAF0.4086
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21760908OA-icon.png] Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population