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rs3809922

From SNPedia

Orientationminus
Stabilizedminus
Make rs3809922(C;C)
Make rs3809922(C;T)
Make rs3809922(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position48921759
GeneSMAD7
is asnp
is mentioned by
dbSNPrs3809922
ebirs3809922
HLIrs3809922
Exacrs3809922
Varsomers3809922
Maprs3809922
PheGenIrs3809922
hapmaprs3809922
1000 genomesrs3809922
hgdprs3809922
ensemblrs3809922
gopubmedrs3809922
geneviewrs3809922
scholarrs3809922
googlers3809922
pharmgkbrs3809922
gwascentralrs3809922
openSNPrs3809922
23andMers3809922
23andMe allrs3809922
SNP Nexus

SNPshotrs3809922
SNPdbers3809922
MSV3drs3809922
GWAS Ctlgrs3809922
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24039762OA-icon.png] Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population