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rs1959122

From SNPedia

Orientationminus
Stabilizedminus
Make rs1959122(A;A)
Make rs1959122(A;G)
Make rs1959122(G;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position81871321
is asnp
is mentioned by
dbSNPrs1959122
ebirs1959122
HLIrs1959122
Exacrs1959122
Varsomers1959122
Maprs1959122
PheGenIrs1959122
hapmaprs1959122
1000 genomesrs1959122
hgdprs1959122
ensemblrs1959122
gopubmedrs1959122
geneviewrs1959122
scholarrs1959122
googlers1959122
pharmgkbrs1959122
gwascentralrs1959122
openSNPrs1959122
23andMers1959122
23andMe allrs1959122
SNP Nexus

SNPshotrs1959122
SNPdbers1959122
MSV3drs1959122
GWAS Ctlgrs1959122
Max Magnitude
? (A;A) (A;G) (G;G) 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 9E-7
Odds Ratio 7.63 [2.92-19.95]