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rs1546498

From SNPedia

Orientationplus
Stabilizedplus
Make rs1546498(C;C)
Make rs1546498(C;T)
Make rs1546498(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position126697272
is asnp
is mentioned by
dbSNPrs1546498
ebirs1546498
HLIrs1546498
Exacrs1546498
Varsomers1546498
Maprs1546498
PheGenIrs1546498
hapmaprs1546498
1000 genomesrs1546498
hgdprs1546498
ensemblrs1546498
gopubmedrs1546498
geneviewrs1546498
scholarrs1546498
googlers1546498
pharmgkbrs1546498
gwascentralrs1546498
openSNPrs1546498
23andMers1546498
23andMe allrs1546498
SNP Nexus

SNPshotrs1546498
SNPdbers1546498
MSV3drs1546498
GWAS Ctlgrs1546498
GMAF0.01102
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 2E-6
Odds Ratio 7.69 [4.57-10.81] unit increase