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rs6788787

From SNPedia

Orientationplus
Make rs6788787(C;C)
Make rs6788787(C;T)
Make rs6788787(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position117152001
is asnp
is mentioned by
dbSNPrs6788787
ebirs6788787
HLIrs6788787
Exacrs6788787
Varsomers6788787
Maprs6788787
PheGenIrs6788787
hapmaprs6788787
1000 genomesrs6788787
hgdprs6788787
ensemblrs6788787
gopubmedrs6788787
geneviewrs6788787
scholarrs6788787
googlers6788787
pharmgkbrs6788787
gwascentralrs6788787
openSNPrs6788787
23andMers6788787
23andMe allrs6788787
SNP Nexus

SNPshotrs6788787
SNPdbers6788787
MSV3drs6788787
GWAS Ctlgrs6788787
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 27187494] Case-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.