rs387906256
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AG;AG) | 0 | common in clinvar |
(GA;GA) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
Make rs387906256(-;-) |
Make rs387906256(-;GA) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 19671810 |
Gene | ALDH3A2 |
is a | snp |
is | mentioned by |
dbSNP | rs387906256 |
dbSNP (classic) | rs387906256 |
ClinGen | rs387906256 |
ebi | rs387906256 |
HLI | rs387906256 |
Exac | rs387906256 |
Gnomad | rs387906256 |
Varsome | rs387906256 |
LitVar | rs387906256 |
Map | rs387906256 |
PheGenI | rs387906256 |
Biobank | rs387906256 |
1000 genomes | rs387906256 |
hgdp | rs387906256 |
ensembl | rs387906256 |
geneview | rs387906256 |
scholar | rs387906256 |
rs387906256 | |
pharmgkb | rs387906256 |
gwascentral | rs387906256 |
openSNP | rs387906256 |
23andMe | rs387906256 |
SNPshot | rs387906256 |
SNPdbe | rs387906256 |
MSV3d | rs387906256 |
GWAS Ctlg | rs387906256 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906256(-;-) Rs387906256(AG;AG) |
Alt | rs387906256(-;-) Rs387906256(AG;AG) |
Reference | Rs387906256(GA;GA) |
Significance | Pathogenic |
Disease | Sjögren-Larsson syndrome not provided |
Variation | info |
Gene | ALDH3A2 |
CLNDBN | Sjögren-Larsson syndrome not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.19575123_19575124delGA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000001708.4, RCV000413153.1, |