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rs863223760

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs863223760
ClinGenrs863223760
ebirs863223760
HLIrs863223760
Exacrs863223760
Gnomadrs863223760
Varsomers863223760
LitVarrs863223760
Maprs863223760
PheGenIrs863223760
Biobankrs863223760
1000 genomesrs863223760
hgdprs863223760
ensemblrs863223760
geneviewrs863223760
scholarrs863223760
googlers863223760
pharmgkbrs863223760
gwascentralrs863223760
openSNPrs863223760
23andMers863223760
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,