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rs863223735

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223735(A;A)
Make rs863223735(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67181264
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223735
ebirs863223735
HLIrs863223735
Exacrs863223735
Varsomers863223735
Maprs863223735
PheGenIrs863223735
hapmaprs863223735
1000 genomesrs863223735
hgdprs863223735
ensemblrs863223735
gopubmedrs863223735
geneviewrs863223735
scholarrs863223735
googlers863223735
pharmgkbrs863223735
gwascentralrs863223735
openSNPrs863223735
23andMers863223735
23andMe allrs863223735
SNP Nexus

SNPshotrs863223735
SNPdbers863223735
MSV3drs863223735
GWAS Ctlgrs863223735
Max Magnitude0
ClinVar
Risk rs863223735(A;A)
Alt rs863223735(A;A)
Reference rs863223735(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SMAD3
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.67473602G>A
CLNSRC
CLNACC RCV000196414.2,