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rs863223737

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223737(A;A)
Make rs863223737(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67181315
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223737
ebirs863223737
HLIrs863223737
Exacrs863223737
Varsomers863223737
Maprs863223737
PheGenIrs863223737
hapmaprs863223737
1000 genomesrs863223737
hgdprs863223737
ensemblrs863223737
gopubmedrs863223737
geneviewrs863223737
scholarrs863223737
googlers863223737
pharmgkbrs863223737
gwascentralrs863223737
openSNPrs863223737
23andMers863223737
23andMe allrs863223737
SNP Nexus

SNPshotrs863223737
SNPdbers863223737
MSV3drs863223737
GWAS Ctlgrs863223737
Max Magnitude0
ClinVar
Risk rs863223737(A;A)
Alt rs863223737(A;A)
Reference rs863223737(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67473653G>A
CLNSRC
CLNACC RCV000199185.1,