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rs863223757

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs863223757(-;-)
Make rs863223757(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67165075
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223757
dbSNP (classic)rs863223757
ClinGenrs863223757
ebirs863223757
HLIrs863223757
Exacrs863223757
Gnomadrs863223757
Varsomers863223757
LitVarrs863223757
Maprs863223757
PheGenIrs863223757
Biobankrs863223757
1000 genomesrs863223757
hgdprs863223757
ensemblrs863223757
geneviewrs863223757
scholarrs863223757
googlers863223757
pharmgkbrs863223757
gwascentralrs863223757
openSNPrs863223757
23andMers863223757
SNPshotrs863223757
SNPdbers863223757
MSV3drs863223757
GWAS Ctlgrs863223757
Max Magnitude0
ClinVar
Risk rs863223757(-;-)
Alt rs863223757(-;-)
Reference Rs863223757(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67457413_67457414delAG
CLNSRC
CLNACC RCV000197979.2,