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rs6751349

From SNPedia

Orientationplus
Stabilizedplus
Make rs6751349(A;A)
Make rs6751349(A;C)
Make rs6751349(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position45949823
GenePRKCE
is asnp
is mentioned by
dbSNPrs6751349
ebirs6751349
HLIrs6751349
Exacrs6751349
Varsomers6751349
Maprs6751349
PheGenIrs6751349
hapmaprs6751349
1000 genomesrs6751349
hgdprs6751349
ensemblrs6751349
gopubmedrs6751349
geneviewrs6751349
scholarrs6751349
googlers6751349
pharmgkbrs6751349
gwascentralrs6751349
openSNPrs6751349
23andMers6751349
23andMe allrs6751349
SNP Nexus

SNPshotrs6751349
SNPdbers6751349
MSV3drs6751349
GWAS Ctlgrs6751349
GMAF0.1483
Max Magnitude
? (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 1.22 [0.69-1.75] unit decrease