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rs6941513

From SNPedia

Orientationplus
Make rs6941513(A;A)
Make rs6941513(A;G)
Make rs6941513(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position163609768
is asnp
is mentioned by
dbSNPrs6941513
ebirs6941513
HLIrs6941513
Exacrs6941513
Varsomers6941513
Maprs6941513
PheGenIrs6941513
hapmaprs6941513
1000 genomesrs6941513
hgdprs6941513
ensemblrs6941513
gopubmedrs6941513
geneviewrs6941513
scholarrs6941513
googlers6941513
pharmgkbrs6941513
gwascentralrs6941513
openSNPrs6941513
23andMers6941513
23andMe allrs6941513
SNP Nexus

SNPshotrs6941513
SNPdbers6941513
MSV3drs6941513
GWAS Ctlgrs6941513
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 26950853] Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.