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rs863223763

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223763(C;T)
Make rs863223763(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67164914
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223763
ebirs863223763
HLIrs863223763
Exacrs863223763
Varsomers863223763
Maprs863223763
PheGenIrs863223763
hapmaprs863223763
1000 genomesrs863223763
hgdprs863223763
ensemblrs863223763
gopubmedrs863223763
geneviewrs863223763
scholarrs863223763
googlers863223763
pharmgkbrs863223763
gwascentralrs863223763
openSNPrs863223763
23andMers863223763
23andMe allrs863223763
SNP Nexus

SNPshotrs863223763
SNPdbers863223763
MSV3drs863223763
GWAS Ctlgrs863223763
Max Magnitude0
ClinVar
Risk rs863223763(T;T)
Alt rs863223763(T;T)
Reference rs863223763(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67457252C>T
CLNSRC
CLNACC RCV000197374.1,