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rs4796119

From SNPedia

Orientationplus
Stabilizedplus
Make rs4796119(C;C)
Make rs4796119(C;T)
Make rs4796119(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position35866084
GeneC17orf66
is asnp
is mentioned by
dbSNPrs4796119
ebirs4796119
HLIrs4796119
Exacrs4796119
Varsomers4796119
Maprs4796119
PheGenIrs4796119
hapmaprs4796119
1000 genomesrs4796119
hgdprs4796119
ensemblrs4796119
gopubmedrs4796119
geneviewrs4796119
scholarrs4796119
googlers4796119
pharmgkbrs4796119
gwascentralrs4796119
openSNPrs4796119
23andMers4796119
23andMe allrs4796119
SNP Nexus

SNPshotrs4796119
SNPdbers4796119
MSV3drs4796119
GWAS Ctlgrs4796119
GMAF0.1212
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23188791OA-icon.png] Genetic polymorphisms associated carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study