rs796052462
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs796052462(A;A) |
Make rs796052462(A;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 14 |
Position | 28767840 |
Gene | FOXG1 |
is a | snp |
is | mentioned by |
dbSNP | rs796052462 |
dbSNP (classic) | rs796052462 |
ClinGen | rs796052462 |
ebi | rs796052462 |
HLI | rs796052462 |
Exac | rs796052462 |
Gnomad | rs796052462 |
Varsome | rs796052462 |
LitVar | rs796052462 |
Map | rs796052462 |
PheGenI | rs796052462 |
Biobank | rs796052462 |
1000 genomes | rs796052462 |
hgdp | rs796052462 |
ensembl | rs796052462 |
geneview | rs796052462 |
scholar | rs796052462 |
rs796052462 | |
pharmgkb | rs796052462 |
gwascentral | rs796052462 |
openSNP | rs796052462 |
23andMe | rs796052462 |
SNPshot | rs796052462 |
SNPdbe | rs796052462 |
MSV3d | rs796052462 |
GWAS Ctlg | rs796052462 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052462(A;A) rs796052462(G;G) |
Alt | rs796052462(A;A) rs796052462(G;G) |
Reference | Rs796052462(C;C) |
Significance | Pathogenic |
Disease | not provided Inborn genetic diseases |
Variation | info |
Gene | FOXG1 |
CLNDBN | not provided Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000014.8:g.29237046C>A; NC_000014.8:g.29237046C>G |
CLNSRC | |
CLNACC | RCV000187456.2, RCV000190704.1, RCV000255136.1, |