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rs863223743

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223743(A;G)
Make rs863223743(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67190535
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223743
ebirs863223743
HLIrs863223743
Exacrs863223743
Varsomers863223743
Maprs863223743
PheGenIrs863223743
hapmaprs863223743
1000 genomesrs863223743
hgdprs863223743
ensemblrs863223743
gopubmedrs863223743
geneviewrs863223743
scholarrs863223743
googlers863223743
pharmgkbrs863223743
gwascentralrs863223743
openSNPrs863223743
23andMers863223743
23andMe allrs863223743
SNP Nexus

SNPshotrs863223743
SNPdbers863223743
MSV3drs863223743
GWAS Ctlgrs863223743
Max Magnitude0
ClinVar
Risk rs863223743(G;G)
Alt rs863223743(G;G)
Reference rs863223743(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67482873A>G
CLNSRC
CLNACC RCV000195507.1,