rs749597090
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs749597090(C;T) |
Make rs749597090(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 14 |
Position | 87945552 |
Gene | GALC |
is a | snp |
is | mentioned by |
dbSNP | rs749597090 |
dbSNP (classic) | rs749597090 |
ClinGen | rs749597090 |
ebi | rs749597090 |
HLI | rs749597090 |
Exac | rs749597090 |
Gnomad | rs749597090 |
Varsome | rs749597090 |
LitVar | rs749597090 |
Map | rs749597090 |
PheGenI | rs749597090 |
Biobank | rs749597090 |
1000 genomes | rs749597090 |
hgdp | rs749597090 |
ensembl | rs749597090 |
geneview | rs749597090 |
scholar | rs749597090 |
rs749597090 | |
pharmgkb | rs749597090 |
gwascentral | rs749597090 |
openSNP | rs749597090 |
23andMe | rs749597090 |
SNPshot | rs749597090 |
SNPdbe | rs749597090 |
MSV3d | rs749597090 |
GWAS Ctlg | rs749597090 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs749597090(T;T) |
Alt | rs749597090(T;T) |
Reference | Rs749597090(C;C) |
Significance | Probable-Pathogenic |
Disease | Galactosylceramide beta-galactosidase deficiency |
Variation | info |
Gene | GALC |
CLNDBN | Galactosylceramide beta-galactosidase deficiency |
Reversed | 0 |
HGVS | NC_000014.8:g.88411896C>T |
CLNSRC | |
CLNACC | RCV000409892.1, |