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rs863223762

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223762(G;T)
Make rs863223762(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67066308
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223762
ebirs863223762
HLIrs863223762
Exacrs863223762
Varsomers863223762
Maprs863223762
PheGenIrs863223762
hapmaprs863223762
1000 genomesrs863223762
hgdprs863223762
ensemblrs863223762
gopubmedrs863223762
geneviewrs863223762
scholarrs863223762
googlers863223762
pharmgkbrs863223762
gwascentralrs863223762
openSNPrs863223762
23andMers863223762
23andMe allrs863223762
SNP Nexus

SNPshotrs863223762
SNPdbers863223762
MSV3drs863223762
GWAS Ctlgrs863223762
Max Magnitude0
ClinVar
Risk rs863223762(T;T)
Alt rs863223762(T;T)
Reference rs863223762(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67358646G>T
CLNSRC
CLNACC RCV000200589.1,