rs794727798
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs794727798(C;T) |
Make rs794727798(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 15 |
Position | 67181384 |
Gene | SMAD3 |
is a | snp |
is | mentioned by |
dbSNP | rs794727798 |
dbSNP (classic) | rs794727798 |
ClinGen | rs794727798 |
ebi | rs794727798 |
HLI | rs794727798 |
Exac | rs794727798 |
Gnomad | rs794727798 |
Varsome | rs794727798 |
LitVar | rs794727798 |
Map | rs794727798 |
PheGenI | rs794727798 |
Biobank | rs794727798 |
1000 genomes | rs794727798 |
hgdp | rs794727798 |
ensembl | rs794727798 |
geneview | rs794727798 |
scholar | rs794727798 |
rs794727798 | |
pharmgkb | rs794727798 |
gwascentral | rs794727798 |
openSNP | rs794727798 |
23andMe | rs794727798 |
SNPshot | rs794727798 |
SNPdbe | rs794727798 |
MSV3d | rs794727798 |
GWAS Ctlg | rs794727798 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794727798(T;T) |
Alt | rs794727798(T;T) |
Reference | Rs794727798(C;C) |
Significance | Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | SMAD3 |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000015.9:g.67473722C>T |
CLNSRC | |
CLNACC | RCV000179456.4, RCV000235212.1, |