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rs6763159

From SNPedia

Orientationplus
Stabilizedplus
Make rs6763159(C;C)
Make rs6763159(C;T)
Make rs6763159(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position59663795
is asnp
is mentioned by
dbSNPrs6763159
ebirs6763159
HLIrs6763159
Exacrs6763159
Varsomers6763159
Maprs6763159
PheGenIrs6763159
hapmaprs6763159
1000 genomesrs6763159
hgdprs6763159
ensemblrs6763159
gopubmedrs6763159
geneviewrs6763159
scholarrs6763159
googlers6763159
pharmgkbrs6763159
gwascentralrs6763159
openSNPrs6763159
23andMers6763159
23andMe allrs6763159
SNP Nexus

SNPshotrs6763159
SNPdbers6763159
MSV3drs6763159
GWAS Ctlgrs6763159
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24800985OA-icon.png]
Trait Conotruncal heart defects
Title Genome-wide association study of maternal and inherited loci for conotruncal heart defects.
Risk Allele
P-val 1E-6
Odds Ratio 1.47 [1.25-1.72]