Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223768

From SNPedia

Orientationplus
Make rs863223768(-;-)
Make rs863223768(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67184797
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223768
ebirs863223768
HLIrs863223768
Exacrs863223768
Varsomers863223768
Maprs863223768
PheGenIrs863223768
hapmaprs863223768
1000 genomesrs863223768
hgdprs863223768
ensemblrs863223768
gopubmedrs863223768
geneviewrs863223768
scholarrs863223768
googlers863223768
pharmgkbrs863223768
gwascentralrs863223768
openSNPrs863223768
23andMers863223768
23andMe allrs863223768
SNP Nexus

SNPshotrs863223768
SNPdbers863223768
MSV3drs863223768
GWAS Ctlgrs863223768
Max Magnitude
ClinVar
Risk rs863223768(;)
Alt rs863223768(;)
Reference rs863223768(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67477135delT
CLNSRC
CLNACC RCV000199350.2,