rs761550284
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | carrier of one Krabbe disease allele |
(T;T) | 6 | Krabbe disease (likely) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 87984487 |
Gene | GALC |
is a | snp |
is | mentioned by |
dbSNP | rs761550284 |
dbSNP (classic) | rs761550284 |
ClinGen | rs761550284 |
ebi | rs761550284 |
HLI | rs761550284 |
Exac | rs761550284 |
Gnomad | rs761550284 |
Varsome | rs761550284 |
LitVar | rs761550284 |
Map | rs761550284 |
PheGenI | rs761550284 |
Biobank | rs761550284 |
1000 genomes | rs761550284 |
hgdp | rs761550284 |
ensembl | rs761550284 |
geneview | rs761550284 |
scholar | rs761550284 |
rs761550284 | |
pharmgkb | rs761550284 |
gwascentral | rs761550284 |
openSNP | rs761550284 |
23andMe | rs761550284 |
SNPshot | rs761550284 |
SNPdbe | rs761550284 |
MSV3d | rs761550284 |
GWAS Ctlg | rs761550284 |
Max Magnitude | 6 |
aka c.489G>A, p.Trp163Ter
Identified in ClinVar as likely pathogenic for Krabbe disease (when inherited in two copies or as a compound heterozygote)
ClinVar | |
---|---|
Risk | Rs761550284(T;T) |
Alt | Rs761550284(T;T) |
Reference | Rs761550284(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.88450831C>T |
CLNSRC | |
CLNACC | RCV000169212.1, |