rs398123177
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 6 | Krabbe disease (likely) |
(C;T) | 3 | carrier of one Krabbe disease allele |
(T;T) | 0 | common in clinvar |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 87968381 |
Gene | GALC |
is a | snp |
is | mentioned by |
dbSNP | rs398123177 |
dbSNP (classic) | rs398123177 |
ClinGen | rs398123177 |
ebi | rs398123177 |
HLI | rs398123177 |
Exac | rs398123177 |
Gnomad | rs398123177 |
Varsome | rs398123177 |
LitVar | rs398123177 |
Map | rs398123177 |
PheGenI | rs398123177 |
Biobank | rs398123177 |
1000 genomes | rs398123177 |
hgdp | rs398123177 |
ensembl | rs398123177 |
geneview | rs398123177 |
scholar | rs398123177 |
rs398123177 | |
pharmgkb | rs398123177 |
gwascentral | rs398123177 |
openSNP | rs398123177 |
23andMe | rs398123177 |
SNPshot | rs398123177 |
SNPdbe | rs398123177 |
MSV3d | rs398123177 |
GWAS Ctlg | rs398123177 |
Max Magnitude | 6 |
aka c.862T>C, p.Trp288Arg
Identified in ClinVar as likely pathogenic for Krabbe disease (when inherited recessively or as a compound heterozygote)
ClinVar | |
---|---|
Risk | Rs398123177(C;C) |
Alt | Rs398123177(C;C) |
Reference | Rs398123177(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided Galactosylceramide beta-galactosidase deficiency |
Variation | info |
Gene | GALC |
CLNDBN | not provided Galactosylceramide beta-galactosidase deficiency |
Reversed | 1 |
HGVS | NC_000014.8:g.88434725A>G |
CLNSRC | ClinVar Emory University |
CLNACC | RCV000078208.3, RCV000180100.1, |