rs367902696
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | Carrier of a biotinidase deficiency mutation |
(G;G) | 0 | common in clinvar |
Make rs367902696(A;A) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 15642041 |
Gene | BTD |
is a | snp |
is | mentioned by |
dbSNP | rs367902696 |
dbSNP (classic) | rs367902696 |
ClinGen | rs367902696 |
ebi | rs367902696 |
HLI | rs367902696 |
Exac | rs367902696 |
Gnomad | rs367902696 |
Varsome | rs367902696 |
LitVar | rs367902696 |
Map | rs367902696 |
PheGenI | rs367902696 |
Biobank | rs367902696 |
1000 genomes | rs367902696 |
hgdp | rs367902696 |
ensembl | rs367902696 |
geneview | rs367902696 |
scholar | rs367902696 |
rs367902696 | |
pharmgkb | rs367902696 |
gwascentral | rs367902696 |
openSNP | rs367902696 |
23andMe | rs367902696 |
SNPshot | rs367902696 |
SNPdbe | rs367902696 |
MSV3d | rs367902696 |
GWAS Ctlg | rs367902696 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs367902696(A;A) |
Alt | rs367902696(A;A) |
Reference | Rs367902696(G;G) |
Significance | Pathogenic |
Disease | Biotinidase deficiency not provided |
Variation | info |
Gene | BTD |
CLNDBN | Biotinidase deficiency not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.15683548G>A |
CLNSRC | ARUP BTD |
CLNACC | RCV000021924.1, RCV000490188.1, |