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rs1676232

From SNPedia

Orientationplus
Stabilizedplus
Make rs1676232(A;A)
Make rs1676232(A;G)
Make rs1676232(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position117515992
GeneLOC105374056
is asnp
is mentioned by
dbSNPrs1676232
dbSNP (classic)rs1676232
ClinGenrs1676232
ebirs1676232
HLIrs1676232
Exacrs1676232
Gnomadrs1676232
Varsomers1676232
LitVarrs1676232
Maprs1676232
PheGenIrs1676232
Biobankrs1676232
1000 genomesrs1676232
hgdprs1676232
ensemblrs1676232
geneviewrs1676232
scholarrs1676232
googlers1676232
pharmgkbrs1676232
gwascentralrs1676232
openSNPrs1676232
23andMers1676232
23andMe allrs1676232
SNPshotrs1676232
SNPdbers1676232
MSV3drs1676232
GWAS Ctlgrs1676232
GMAF0.4013
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 18318786OA-icon.png],AEHA 2008 ppt - rs4404477(A)/rs1676232(A) defines a significant left main coronary artery disease risk haplotype