rs759874793
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs759874793(A;A) |
Make rs759874793(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 19651627 |
Gene | ALDH3A2 |
is a | snp |
is | mentioned by |
dbSNP | rs759874793 |
dbSNP (classic) | rs759874793 |
ClinGen | rs759874793 |
ebi | rs759874793 |
HLI | rs759874793 |
Exac | rs759874793 |
Gnomad | rs759874793 |
Varsome | rs759874793 |
LitVar | rs759874793 |
Map | rs759874793 |
PheGenI | rs759874793 |
Biobank | rs759874793 |
1000 genomes | rs759874793 |
hgdp | rs759874793 |
ensembl | rs759874793 |
geneview | rs759874793 |
scholar | rs759874793 |
rs759874793 | |
pharmgkb | rs759874793 |
gwascentral | rs759874793 |
openSNP | rs759874793 |
23andMe | rs759874793 |
SNPshot | rs759874793 |
SNPdbe | rs759874793 |
MSV3d | rs759874793 |
GWAS Ctlg | rs759874793 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759874793(A;A) rs759874793(C;C) |
Alt | rs759874793(A;A) rs759874793(C;C) |
Reference | Rs759874793(G;G) |
Significance | Probable-Pathogenic |
Disease | Sjögren-Larsson syndrome |
Variation | info |
Gene | ALDH3A2 |
CLNDBN | Sjögren-Larsson syndrome |
Reversed | 0 |
HGVS | NC_000017.10:g.19554940G>A |
CLNSRC | |
CLNACC | RCV000410260.1, |