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rs11872184

From SNPedia

Orientationplus
Stabilizedplus
Make rs11872184(A;A)
Make rs11872184(A;G)
Make rs11872184(G;G)
ReferenceGRCh38 38.1/142
Chromosome18
Position2739735
GeneSMCHD1
is asnp
is mentioned by
dbSNPrs11872184
ebirs11872184
HLIrs11872184
Exacrs11872184
Varsomers11872184
Maprs11872184
PheGenIrs11872184
hapmaprs11872184
1000 genomesrs11872184
hgdprs11872184
ensemblrs11872184
gopubmedrs11872184
geneviewrs11872184
scholarrs11872184
googlers11872184
pharmgkbrs11872184
gwascentralrs11872184
openSNPrs11872184
23andMers11872184
23andMe allrs11872184
SNP Nexus

SNPshotrs11872184
SNPdbers11872184
MSV3drs11872184
GWAS Ctlgrs11872184
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 4E-6
Odds Ratio 4.08 [2.15-7.74]