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rs9342616

From SNPedia

Orientationplus
Stabilizedplus
Make rs9342616(A;A)
Make rs9342616(A;G)
Make rs9342616(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position67176026
is asnp
is mentioned by
dbSNPrs9342616
dbSNP (classic)rs9342616
ClinGenrs9342616
ebirs9342616
HLIrs9342616
Exacrs9342616
Gnomadrs9342616
Varsomers9342616
LitVarrs9342616
Maprs9342616
PheGenIrs9342616
Biobankrs9342616
1000 genomesrs9342616
hgdprs9342616
ensemblrs9342616
geneviewrs9342616
scholarrs9342616
googlers9342616
pharmgkbrs9342616
gwascentralrs9342616
openSNPrs9342616
23andMers9342616
SNPshotrs9342616
SNPdbers9342616
MSV3drs9342616
GWAS Ctlgrs9342616
GMAF0.3834
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23534349OA-icon.png]
Trait QT interval
Title Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
Risk Allele A
P-val 1E-6
Odds Ratio 6.92 [NR] ms decrease