Have questions? Visit https://www.reddit.com/r/SNPedia

rs11017328

From SNPedia

Orientationplus
Stabilizedplus
Make rs11017328(C;C)
Make rs11017328(C;T)
Make rs11017328(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position130548836
is asnp
is mentioned by
dbSNPrs11017328
ebirs11017328
HLIrs11017328
Exacrs11017328
Varsomers11017328
Maprs11017328
PheGenIrs11017328
hapmaprs11017328
1000 genomesrs11017328
hgdprs11017328
ensemblrs11017328
gopubmedrs11017328
geneviewrs11017328
scholarrs11017328
googlers11017328
pharmgkbrs11017328
gwascentralrs11017328
openSNPrs11017328
23andMers11017328
23andMe allrs11017328
SNP Nexus

SNPshotrs11017328
SNPdbers11017328
MSV3drs11017328
GWAS Ctlgrs11017328
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 3E-7
Odds Ratio 2.87 [1.88-4.40]