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rs6894385

From SNPedia

Orientationplus
Stabilizedplus
Make rs6894385(A;A)
Make rs6894385(A;C)
Make rs6894385(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position73981078
is asnp
is mentioned by
dbSNPrs6894385
ebirs6894385
HLIrs6894385
Exacrs6894385
Varsomers6894385
Maprs6894385
PheGenIrs6894385
hapmaprs6894385
1000 genomesrs6894385
hgdprs6894385
ensemblrs6894385
gopubmedrs6894385
geneviewrs6894385
scholarrs6894385
googlers6894385
pharmgkbrs6894385
gwascentralrs6894385
openSNPrs6894385
23andMers6894385
23andMe allrs6894385
SNP Nexus

SNPshotrs6894385
SNPdbers6894385
MSV3drs6894385
GWAS Ctlgrs6894385
GMAF0.1731
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 1E-6
Odds Ratio 9.92 [NR] ms decrease