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

rs863223759

From SNPedia

Orientationplus
Make rs863223759(-;-)
Make rs863223759(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67165307
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223759
ebirs863223759
HLIrs863223759
Exacrs863223759
Varsomers863223759
Maprs863223759
PheGenIrs863223759
hapmaprs863223759
1000 genomesrs863223759
hgdprs863223759
ensemblrs863223759
gopubmedrs863223759
geneviewrs863223759
scholarrs863223759
googlers863223759
pharmgkbrs863223759
gwascentralrs863223759
openSNPrs863223759
23andMers863223759
23andMe allrs863223759
SNP Nexus

SNPshotrs863223759
SNPdbers863223759
MSV3drs863223759
GWAS Ctlgrs863223759
Max Magnitude
ClinVar
Risk rs863223759(;)
Alt rs863223759(;)
Reference rs863223759(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.67457645delC
CLNSRC
CLNACC RCV000196308.2,