rs3729856
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs3729856(A;G) |
Make rs3729856(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 11757066 |
Gene | GATA4 |
is a | snp |
is | mentioned by |
dbSNP | rs3729856 |
dbSNP (classic) | rs3729856 |
ClinGen | rs3729856 |
ebi | rs3729856 |
HLI | rs3729856 |
Exac | rs3729856 |
Gnomad | rs3729856 |
Varsome | rs3729856 |
LitVar | rs3729856 |
Map | rs3729856 |
PheGenI | rs3729856 |
Biobank | rs3729856 |
1000 genomes | rs3729856 |
hgdp | rs3729856 |
ensembl | rs3729856 |
geneview | rs3729856 |
scholar | rs3729856 |
rs3729856 | |
pharmgkb | rs3729856 |
gwascentral | rs3729856 |
openSNP | rs3729856 |
23andMe | rs3729856 |
SNPshot | rs3729856 |
SNPdbe | rs3729856 |
MSV3d | rs3729856 |
GWAS Ctlg | rs3729856 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs3729856(G;G) |
Alt | rs3729856(G;G) |
Reference | Rs3729856(A;A) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | GATA4 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000008.10:g.11614575A>G |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000037322.2, RCV000128527.1, |