rs864321699
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs864321699(A;A) |
Make rs864321699(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 11708337 |
Gene | GATA4 |
is a | snp |
is | mentioned by |
dbSNP | rs864321699 |
dbSNP (classic) | rs864321699 |
ClinGen | rs864321699 |
ebi | rs864321699 |
HLI | rs864321699 |
Exac | rs864321699 |
Gnomad | rs864321699 |
Varsome | rs864321699 |
LitVar | rs864321699 |
Map | rs864321699 |
PheGenI | rs864321699 |
Biobank | rs864321699 |
1000 genomes | rs864321699 |
hgdp | rs864321699 |
ensembl | rs864321699 |
geneview | rs864321699 |
scholar | rs864321699 |
rs864321699 | |
pharmgkb | rs864321699 |
gwascentral | rs864321699 |
openSNP | rs864321699 |
23andMe | rs864321699 |
SNPshot | rs864321699 |
SNPdbe | rs864321699 |
MSV3d | rs864321699 |
GWAS Ctlg | rs864321699 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs864321699(A;A) |
Alt | rs864321699(A;A) |
Reference | Rs864321699(G;G) |
Significance | Pathogenic |
Disease | Congenital heart disease |
Variation | info |
Gene | GATA4 |
CLNDBN | Congenital heart disease |
Reversed | 0 |
HGVS | NC_000008.10:g.11565846G>A |
CLNSRC | |
CLNACC | RCV000203597.1, |