rs786204625
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs786204625(-;-) |
Make rs786204625(-;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 19663492 |
Gene | ALDH3A2 |
is a | snp |
is | mentioned by |
dbSNP | rs786204625 |
dbSNP (classic) | rs786204625 |
ClinGen | rs786204625 |
ebi | rs786204625 |
HLI | rs786204625 |
Exac | rs786204625 |
Gnomad | rs786204625 |
Varsome | rs786204625 |
LitVar | rs786204625 |
Map | rs786204625 |
PheGenI | rs786204625 |
Biobank | rs786204625 |
1000 genomes | rs786204625 |
hgdp | rs786204625 |
ensembl | rs786204625 |
geneview | rs786204625 |
scholar | rs786204625 |
rs786204625 | |
pharmgkb | rs786204625 |
gwascentral | rs786204625 |
openSNP | rs786204625 |
23andMe | rs786204625 |
SNPshot | rs786204625 |
SNPdbe | rs786204625 |
MSV3d | rs786204625 |
GWAS Ctlg | rs786204625 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786204625(-;-) |
Alt | rs786204625(-;-) |
Reference | Rs786204625(A;A) |
Significance | Probable-Pathogenic |
Disease | Sjögren-Larsson syndrome |
Variation | info |
Gene | ALDH3A2 |
CLNDBN | Sjögren-Larsson syndrome |
Reversed | 0 |
HGVS | NC_000017.10:g.19566805delA |
CLNSRC | |
CLNACC | RCV000169395.1, |