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rs3809923

From SNPedia

Orientationminus
Stabilizedminus
Make rs3809923(C;C)
Make rs3809923(C;G)
Make rs3809923(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position48921447
GeneSMAD7
is asnp
is mentioned by
dbSNPrs3809923
ebirs3809923
HLIrs3809923
Exacrs3809923
Varsomers3809923
Maprs3809923
PheGenIrs3809923
hapmaprs3809923
1000 genomesrs3809923
hgdprs3809923
ensemblrs3809923
gopubmedrs3809923
geneviewrs3809923
scholarrs3809923
googlers3809923
pharmgkbrs3809923
gwascentralrs3809923
openSNPrs3809923
23andMers3809923
23andMe allrs3809923
SNP Nexus

SNPshotrs3809923
SNPdbers3809923
MSV3drs3809923
GWAS Ctlgrs3809923
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 24039762OA-icon.png] Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population