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rs863223761

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223761(C;C)
Make rs863223761(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67181455
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223761
ebirs863223761
HLIrs863223761
Exacrs863223761
Varsomers863223761
Maprs863223761
PheGenIrs863223761
hapmaprs863223761
1000 genomesrs863223761
hgdprs863223761
ensemblrs863223761
gopubmedrs863223761
geneviewrs863223761
scholarrs863223761
googlers863223761
pharmgkbrs863223761
gwascentralrs863223761
openSNPrs863223761
23andMers863223761
23andMe allrs863223761
SNP Nexus

SNPshotrs863223761
SNPdbers863223761
MSV3drs863223761
GWAS Ctlgrs863223761
Max Magnitude0
ClinVar
Risk rs863223761(C;C)
Alt rs863223761(C;C)
Reference rs863223761(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67473793T>C
CLNSRC
CLNACC RCV000196139.1,