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rs16976171

From SNPedia

Orientationplus
Stabilizedplus
Make rs16976171(G;G)
Make rs16976171(G;T)
Make rs16976171(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position42479656
GeneLINC00907
is asnp
is mentioned by
dbSNPrs16976171
ebirs16976171
HLIrs16976171
Exacrs16976171
Varsomers16976171
Maprs16976171
PheGenIrs16976171
hapmaprs16976171
1000 genomesrs16976171
hgdprs16976171
ensemblrs16976171
gopubmedrs16976171
geneviewrs16976171
scholarrs16976171
googlers16976171
pharmgkbrs16976171
gwascentralrs16976171
openSNPrs16976171
23andMers16976171
23andMe allrs16976171
SNP Nexus

SNPshotrs16976171
SNPdbers16976171
MSV3drs16976171
GWAS Ctlgrs16976171
GMAF0.05326
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23870195OA-icon.png]
Trait Coronary artery calcification
Title Genetics of coronary artery calcification among African Americans, a meta-analysis.
Risk Allele T
P-val 4E-6
Odds Ratio .20 [0.12-0.28] unit decrease