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rs6545278

From SNPedia

Orientationplus
Stabilizedplus
Make rs6545278(G;G)
Make rs6545278(G;T)
Make rs6545278(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position52478914
is asnp
is mentioned by
dbSNPrs6545278
ebirs6545278
HLIrs6545278
Exacrs6545278
Varsomers6545278
Maprs6545278
PheGenIrs6545278
hapmaprs6545278
1000 genomesrs6545278
hgdprs6545278
ensemblrs6545278
gopubmedrs6545278
geneviewrs6545278
scholarrs6545278
googlers6545278
pharmgkbrs6545278
gwascentralrs6545278
openSNPrs6545278
23andMers6545278
23andMe allrs6545278
SNP Nexus

SNPshotrs6545278
SNPdbers6545278
MSV3drs6545278
GWAS Ctlgrs6545278
Max Magnitude
? (G;G) (G;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 8E-7
Odds Ratio 2.62 [1.76-3.90]