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rs746265

From SNPedia

Orientationplus
Stabilizedplus
Make rs746265(A;A)
Make rs746265(A;C)
Make rs746265(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position39284359
is asnp
is mentioned by
dbSNPrs746265
ebirs746265
HLIrs746265
Exacrs746265
Varsomers746265
Maprs746265
PheGenIrs746265
hapmaprs746265
1000 genomesrs746265
hgdprs746265
ensemblrs746265
gopubmedrs746265
geneviewrs746265
scholarrs746265
googlers746265
pharmgkbrs746265
gwascentralrs746265
openSNPrs746265
23andMers746265
23andMe allrs746265
SNP Nexus

SNPshotrs746265
SNPdbers746265
MSV3drs746265
GWAS Ctlgrs746265
GMAF0.1497
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23534349OA-icon.png]
Trait PR interval
Title Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
Risk Allele C
P-val 8E-6
Odds Ratio 6.27 [NR] ms decrease