rs201948406
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs201948406(C;T) |
Make rs201948406(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 5 |
Position | 126568296 |
Gene | ALDH7A1 |
is a | snp |
is | mentioned by |
dbSNP | rs201948406 |
dbSNP (classic) | rs201948406 |
ClinGen | rs201948406 |
ebi | rs201948406 |
HLI | rs201948406 |
Exac | rs201948406 |
Gnomad | rs201948406 |
Varsome | rs201948406 |
LitVar | rs201948406 |
Map | rs201948406 |
PheGenI | rs201948406 |
Biobank | rs201948406 |
1000 genomes | rs201948406 |
hgdp | rs201948406 |
ensembl | rs201948406 |
geneview | rs201948406 |
scholar | rs201948406 |
rs201948406 | |
pharmgkb | rs201948406 |
gwascentral | rs201948406 |
openSNP | rs201948406 |
23andMe | rs201948406 |
SNPshot | rs201948406 |
SNPdbe | rs201948406 |
MSV3d | rs201948406 |
GWAS Ctlg | rs201948406 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201948406(A;A) rs201948406(G;G) rs201948406(T;T) |
Alt | rs201948406(A;A) rs201948406(G;G) rs201948406(T;T) |
Reference | Rs201948406(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ALDH7A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.125903988C>T |
CLNSRC | |
CLNACC | RCV000255917.2, |