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rs6861497

From SNPedia

Orientationplus
Stabilizedplus
Make rs6861497(A;A)
Make rs6861497(A;G)
Make rs6861497(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position102067882
is asnp
is mentioned by
dbSNPrs6861497
dbSNP (classic)rs6861497
ClinGenrs6861497
ebirs6861497
HLIrs6861497
Exacrs6861497
Gnomadrs6861497
Varsomers6861497
LitVarrs6861497
Maprs6861497
PheGenIrs6861497
Biobankrs6861497
1000 genomesrs6861497
hgdprs6861497
ensemblrs6861497
geneviewrs6861497
scholarrs6861497
googlers6861497
pharmgkbrs6861497
gwascentralrs6861497
openSNPrs6861497
23andMers6861497
SNPshotrs6861497
SNPdbers6861497
MSV3drs6861497
GWAS Ctlgrs6861497
GMAF0.4045
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23534349OA-icon.png]
Trait QRS duration
Title Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
Risk Allele A
P-val 5E-6
Odds Ratio 2.34 [NR] ms increase