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rs1263163

From SNPedia

Orientationplus
Stabilizedplus
Make rs1263163(A;A)
Make rs1263163(A;G)
Make rs1263163(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position116802796
is asnp
is mentioned by
dbSNPrs1263163
dbSNP (old)rs1263163
ClinGenrs1263163
ebirs1263163
HLIrs1263163
Exacrs1263163
Gnomadrs1263163
Varsomers1263163
Maprs1263163
PheGenIrs1263163
Biobankrs1263163
1000 genomesrs1263163
hgdprs1263163
ensemblrs1263163
gopubmedrs1263163
geneviewrs1263163
scholarrs1263163
googlers1263163
pharmgkbrs1263163
gwascentralrs1263163
openSNPrs1263163
23andMers1263163
23andMe allrs1263163
SNPshotrs1263163
SNPdbers1263163
MSV3drs1263163
GWAS Ctlgrs1263163
Max Magnitude
? (A;A) (A;G) (G;G) 28

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

[PMID 28610615OA-icon.png] Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India.