rs863223759
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs863223759(-;-) |
Make rs863223759(-;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 67165307 |
Gene | SMAD3 |
is a | snp |
is | mentioned by |
dbSNP | rs863223759 |
dbSNP (classic) | rs863223759 |
ClinGen | rs863223759 |
ebi | rs863223759 |
HLI | rs863223759 |
Exac | rs863223759 |
Gnomad | rs863223759 |
Varsome | rs863223759 |
LitVar | rs863223759 |
Map | rs863223759 |
PheGenI | rs863223759 |
Biobank | rs863223759 |
1000 genomes | rs863223759 |
hgdp | rs863223759 |
ensembl | rs863223759 |
geneview | rs863223759 |
scholar | rs863223759 |
rs863223759 | |
pharmgkb | rs863223759 |
gwascentral | rs863223759 |
openSNP | rs863223759 |
23andMe | rs863223759 |
SNPshot | rs863223759 |
SNPdbe | rs863223759 |
MSV3d | rs863223759 |
GWAS Ctlg | rs863223759 |
Max Magnitude | 0 |
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 | RCV000196308.3, |