rs786205005
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs786205005(A;A) |
Make rs786205005(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 14 |
Position | 28767856 |
Gene | FOXG1 |
is a | snp |
is | mentioned by |
dbSNP | rs786205005 |
dbSNP (classic) | rs786205005 |
ClinGen | rs786205005 |
ebi | rs786205005 |
HLI | rs786205005 |
Exac | rs786205005 |
Gnomad | rs786205005 |
Varsome | rs786205005 |
LitVar | rs786205005 |
Map | rs786205005 |
PheGenI | rs786205005 |
Biobank | rs786205005 |
1000 genomes | rs786205005 |
hgdp | rs786205005 |
ensembl | rs786205005 |
geneview | rs786205005 |
scholar | rs786205005 |
rs786205005 | |
pharmgkb | rs786205005 |
gwascentral | rs786205005 |
openSNP | rs786205005 |
23andMe | rs786205005 |
SNPshot | rs786205005 |
SNPdbe | rs786205005 |
MSV3d | rs786205005 |
GWAS Ctlg | rs786205005 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205005(A;A) |
Alt | rs786205005(A;A) |
Reference | Rs786205005(G;G) |
Significance | Pathogenic |
Disease | Rett syndrome |
Variation | info |
Gene | FOXG1 |
CLNDBN | Rett syndrome, congenital variant |
Reversed | 0 |
HGVS | NC_000014.8:g.29237062G>A |
CLNSRC | |
CLNACC | RCV000170078.1, |