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rs6788787

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs6788787
ClinGenrs6788787
ebirs6788787
HLIrs6788787
Exacrs6788787
Gnomadrs6788787
Varsomers6788787
LitVarrs6788787
Maprs6788787
PheGenIrs6788787
Biobankrs6788787
1000 genomesrs6788787
hgdprs6788787
ensemblrs6788787
geneviewrs6788787
scholarrs6788787
googlers6788787
pharmgkbrs6788787
gwascentralrs6788787
openSNPrs6788787
23andMers6788787
SNPshotrs6788787
SNPdbers6788787
MSV3drs6788787
GWAS Ctlgrs6788787
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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