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rs863223760

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223760(-;T)
Make rs863223760(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67165344
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223760
ClinGenrs863223760
ebirs863223760
HLIrs863223760
Exacrs863223760
Varsomers863223760
Maprs863223760
PheGenIrs863223760
hapmaprs863223760
1000 genomesrs863223760
hgdprs863223760
ensemblrs863223760
gopubmedrs863223760
geneviewrs863223760
scholarrs863223760
googlers863223760
pharmgkbrs863223760
gwascentralrs863223760
openSNPrs863223760
23andMers863223760
23andMe allrs863223760
SNP Nexus

SNPshotrs863223760
SNPdbers863223760
MSV3drs863223760
GWAS Ctlgrs863223760
Max Magnitude0
ClinVar
Risk rs863223760(T;T)
Alt rs863223760(T;T)
Reference Rs863223760(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67457682dupT
CLNSRC
CLNACC RCV000198497.1,