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rs9866825

From SNPedia

Orientationplus
Stabilizedplus
Make rs9866825(A;A)
Make rs9866825(A;C)
Make rs9866825(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position8209103
is asnp
is mentioned by
dbSNPrs9866825
dbSNP (classic)rs9866825
ClinGenrs9866825
ebirs9866825
HLIrs9866825
Exacrs9866825
Gnomadrs9866825
Varsomers9866825
LitVarrs9866825
Maprs9866825
PheGenIrs9866825
Biobankrs9866825
1000 genomesrs9866825
hgdprs9866825
ensemblrs9866825
geneviewrs9866825
scholarrs9866825
googlers9866825
pharmgkbrs9866825
gwascentralrs9866825
openSNPrs9866825
23andMers9866825
SNPshotrs9866825
SNPdbers9866825
MSV3drs9866825
GWAS Ctlgrs9866825
GMAF0.3999
Max Magnitude0
? (A;A) (A;C) (C;C) 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 8E-6
Odds Ratio 1.18 [0.67-1.69] unit increase