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rs863223741

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223741(C;C)
Make rs863223741(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67181403
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223741
ebirs863223741
HLIrs863223741
Exacrs863223741
Varsomers863223741
Maprs863223741
PheGenIrs863223741
hapmaprs863223741
1000 genomesrs863223741
hgdprs863223741
ensemblrs863223741
gopubmedrs863223741
geneviewrs863223741
scholarrs863223741
googlers863223741
pharmgkbrs863223741
gwascentralrs863223741
openSNPrs863223741
23andMers863223741
23andMe allrs863223741
SNP Nexus

SNPshotrs863223741
SNPdbers863223741
MSV3drs863223741
GWAS Ctlgrs863223741
Max Magnitude0
ClinVar
Risk rs863223741(C;C)
Alt rs863223741(C;C)
Reference rs863223741(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67473741T>C
CLNSRC
CLNACC RCV000198868.1,