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rs863223770

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223770(-;A)
Make rs863223770(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67164951
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223770
ClinGenrs863223770
ebirs863223770
HLIrs863223770
Exacrs863223770
Varsomers863223770
Maprs863223770
PheGenIrs863223770
hapmaprs863223770
1000 genomesrs863223770
hgdprs863223770
ensemblrs863223770
gopubmedrs863223770
geneviewrs863223770
scholarrs863223770
googlers863223770
pharmgkbrs863223770
gwascentralrs863223770
openSNPrs863223770
23andMers863223770
23andMe allrs863223770
SNP Nexus

SNPshotrs863223770
SNPdbers863223770
MSV3drs863223770
GWAS Ctlgrs863223770
Max Magnitude0
ClinVar
Risk rs863223770(A;A)
Alt rs863223770(A;A)
Reference Rs863223770(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67457289dupA
CLNSRC
CLNACC RCV000197660.1,