rs886042645
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Chromosome | 14 |
Position | 87968411 |
Gene | GALC |
is a | snp |
is | mentioned by |
dbSNP | rs886042645 |
dbSNP (classic) | rs886042645 |
ClinGen | rs886042645 |
ebi | rs886042645 |
HLI | rs886042645 |
Exac | rs886042645 |
Gnomad | rs886042645 |
Varsome | rs886042645 |
LitVar | rs886042645 |
Map | rs886042645 |
PheGenI | rs886042645 |
Biobank | rs886042645 |
1000 genomes | rs886042645 |
hgdp | rs886042645 |
ensembl | rs886042645 |
geneview | rs886042645 |
scholar | rs886042645 |
rs886042645 | |
pharmgkb | rs886042645 |
gwascentral | rs886042645 |
openSNP | rs886042645 |
23andMe | rs886042645 |
SNPshot | rs886042645 |
SNPdbe | rs886042645 |
MSV3d | rs886042645 |
GWAS Ctlg | rs886042645 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886042645(G;G) |
Alt | rs886042645(G;G) |
Reference | Rs886042645(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GALC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.88434755T>G |
CLNSRC | |
CLNACC | RCV000398980.1, |