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rs1263171

From SNPedia

Orientationplus
Stabilizedplus
Make rs1263171(A;A)
Make rs1263171(A;G)
Make rs1263171(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position116809614
is asnp
is mentioned by
dbSNPrs1263171
dbSNP (classic)rs1263171
ClinGenrs1263171
ebirs1263171
HLIrs1263171
Exacrs1263171
Gnomadrs1263171
Varsomers1263171
LitVarrs1263171
Maprs1263171
PheGenIrs1263171
Biobankrs1263171
1000 genomesrs1263171
hgdprs1263171
ensemblrs1263171
geneviewrs1263171
scholarrs1263171
googlers1263171
pharmgkbrs1263171
gwascentralrs1263171
openSNPrs1263171
23andMers1263171
23andMe allrs1263171
SNPshotrs1263171
SNPdbers1263171
MSV3drs1263171
GWAS Ctlgrs1263171
Max Magnitude

[PMID 28257648OA-icon.png] Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India.