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rs863223739

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223739(C;G)
Make rs863223739(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67181369
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223739
ebirs863223739
HLIrs863223739
Exacrs863223739
Varsomers863223739
Maprs863223739
PheGenIrs863223739
hapmaprs863223739
1000 genomesrs863223739
hgdprs863223739
ensemblrs863223739
gopubmedrs863223739
geneviewrs863223739
scholarrs863223739
googlers863223739
pharmgkbrs863223739
gwascentralrs863223739
openSNPrs863223739
23andMers863223739
23andMe allrs863223739
SNP Nexus

SNPshotrs863223739
SNPdbers863223739
MSV3drs863223739
GWAS Ctlgrs863223739
Max Magnitude0
ClinVar
Risk rs863223739(G;G)
Alt rs863223739(G;G)
Reference rs863223739(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67473707C>G
CLNSRC
CLNACC RCV000196773.1,