rs376917645
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs376917645(A;A) |
Make rs376917645(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 5 |
Position | 126577154 |
Gene | ALDH7A1 |
is a | snp |
is | mentioned by |
dbSNP | rs376917645 |
dbSNP (classic) | rs376917645 |
ClinGen | rs376917645 |
ebi | rs376917645 |
HLI | rs376917645 |
Exac | rs376917645 |
Gnomad | rs376917645 |
Varsome | rs376917645 |
LitVar | rs376917645 |
Map | rs376917645 |
PheGenI | rs376917645 |
Biobank | rs376917645 |
1000 genomes | rs376917645 |
hgdp | rs376917645 |
ensembl | rs376917645 |
geneview | rs376917645 |
scholar | rs376917645 |
rs376917645 | |
pharmgkb | rs376917645 |
gwascentral | rs376917645 |
openSNP | rs376917645 |
23andMe | rs376917645 |
SNPshot | rs376917645 |
SNPdbe | rs376917645 |
MSV3d | rs376917645 |
GWAS Ctlg | rs376917645 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs376917645(A;A) |
Alt | rs376917645(A;A) |
Reference | Rs376917645(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ALDH7A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.125912846G>A |
CLNSRC | |
CLNACC | RCV000255618.1, |