rs864321705
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs864321705(G;G) |
Make rs864321705(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 11755135 |
Gene | GATA4 |
is a | snp |
is | mentioned by |
dbSNP | rs864321705 |
dbSNP (classic) | rs864321705 |
ClinGen | rs864321705 |
ebi | rs864321705 |
HLI | rs864321705 |
Exac | rs864321705 |
Gnomad | rs864321705 |
Varsome | rs864321705 |
LitVar | rs864321705 |
Map | rs864321705 |
PheGenI | rs864321705 |
Biobank | rs864321705 |
1000 genomes | rs864321705 |
hgdp | rs864321705 |
ensembl | rs864321705 |
geneview | rs864321705 |
scholar | rs864321705 |
rs864321705 | |
pharmgkb | rs864321705 |
gwascentral | rs864321705 |
openSNP | rs864321705 |
23andMe | rs864321705 |
SNPshot | rs864321705 |
SNPdbe | rs864321705 |
MSV3d | rs864321705 |
GWAS Ctlg | rs864321705 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs864321705(G;G) |
Alt | rs864321705(G;G) |
Reference | Rs864321705(T;T) |
Significance | Pathogenic |
Disease | Congenital heart disease |
Variation | info |
Gene | GATA4 |
CLNDBN | Congenital heart disease |
Reversed | 0 |
HGVS | NC_000008.10:g.11612644T>G |
CLNSRC | |
CLNACC | RCV000203595.1, |