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rs11008099

From SNPedia

Orientationplus
Stabilizedplus
Make rs11008099(A;A)
Make rs11008099(A;G)
Make rs11008099(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position30545703
is asnp
is mentioned by
dbSNPrs11008099
ebirs11008099
HLIrs11008099
Exacrs11008099
Varsomers11008099
Maprs11008099
PheGenIrs11008099
hapmaprs11008099
1000 genomesrs11008099
hgdprs11008099
ensemblrs11008099
gopubmedrs11008099
geneviewrs11008099
scholarrs11008099
googlers11008099
pharmgkbrs11008099
gwascentralrs11008099
openSNPrs11008099
23andMers11008099
23andMe allrs11008099
SNP Nexus

SNPshotrs11008099
SNPdbers11008099
MSV3drs11008099
GWAS Ctlgrs11008099
GMAF0.1028
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23166209OA-icon.png]
Trait QT interval
Title Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
Risk Allele A
P-val 9E-6
Odds Ratio 2.74 [1.54-3.94] unit increase