rs769031989
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs769031989(A;A) |
Make rs769031989(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 42322464 |
Gene | STAT3 |
is a | snp |
is | mentioned by |
dbSNP | rs769031989 |
dbSNP (classic) | rs769031989 |
ClinGen | rs769031989 |
ebi | rs769031989 |
HLI | rs769031989 |
Exac | rs769031989 |
Gnomad | rs769031989 |
Varsome | rs769031989 |
LitVar | rs769031989 |
Map | rs769031989 |
PheGenI | rs769031989 |
Biobank | rs769031989 |
1000 genomes | rs769031989 |
hgdp | rs769031989 |
ensembl | rs769031989 |
geneview | rs769031989 |
scholar | rs769031989 |
rs769031989 | |
pharmgkb | rs769031989 |
gwascentral | rs769031989 |
openSNP | rs769031989 |
23andMe | rs769031989 |
SNPshot | rs769031989 |
SNPdbe | rs769031989 |
MSV3d | rs769031989 |
GWAS Ctlg | rs769031989 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs769031989(A;A) |
Alt | rs769031989(A;A) |
Reference | Rs769031989(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | STAT3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.40474482T>A |
CLNSRC | |
CLNACC | RCV000414550.1, |