Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223746

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223746(C;T)
Make rs863223746(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67187472
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223746
ebirs863223746
HLIrs863223746
Exacrs863223746
Varsomers863223746
Maprs863223746
PheGenIrs863223746
hapmaprs863223746
1000 genomesrs863223746
hgdprs863223746
ensemblrs863223746
gopubmedrs863223746
geneviewrs863223746
scholarrs863223746
googlers863223746
pharmgkbrs863223746
gwascentralrs863223746
openSNPrs863223746
23andMers863223746
23andMe allrs863223746
SNP Nexus

SNPshotrs863223746
SNPdbers863223746
MSV3drs863223746
GWAS Ctlgrs863223746
Max Magnitude0
ClinVar
Risk rs863223746(T;T)
Alt rs863223746(T;T)
Reference rs863223746(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67479810C>T
CLNSRC
CLNACC RCV000199856.1,