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rs17155315

From SNPedia

Orientationplus
Stabilizedplus
Make rs17155315(A;A)
Make rs17155315(A;G)
Make rs17155315(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position103423957
is asnp
is mentioned by
dbSNPrs17155315
ebirs17155315
HLIrs17155315
Exacrs17155315
Varsomers17155315
Maprs17155315
PheGenIrs17155315
hapmaprs17155315
1000 genomesrs17155315
hgdprs17155315
ensemblrs17155315
gopubmedrs17155315
geneviewrs17155315
scholarrs17155315
googlers17155315
pharmgkbrs17155315
gwascentralrs17155315
openSNPrs17155315
23andMers17155315
23andMe allrs17155315
SNP Nexus

SNPshotrs17155315
SNPdbers17155315
MSV3drs17155315
GWAS Ctlgrs17155315
GMAF0.0202
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 7E-6
Odds Ratio 4.73 [2.69-6.77] unit increase