rs201348482
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201348482(A;A) |
Make rs201348482(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 45603107 |
Gene | BLOC1S6 |
is a | snp |
is | mentioned by |
dbSNP | rs201348482 |
dbSNP (classic) | rs201348482 |
ClinGen | rs201348482 |
ebi | rs201348482 |
HLI | rs201348482 |
Exac | rs201348482 |
Gnomad | rs201348482 |
Varsome | rs201348482 |
LitVar | rs201348482 |
Map | rs201348482 |
PheGenI | rs201348482 |
Biobank | rs201348482 |
1000 genomes | rs201348482 |
hgdp | rs201348482 |
ensembl | rs201348482 |
geneview | rs201348482 |
scholar | rs201348482 |
rs201348482 | |
pharmgkb | rs201348482 |
gwascentral | rs201348482 |
openSNP | rs201348482 |
23andMe | rs201348482 |
SNPshot | rs201348482 |
SNPdbe | rs201348482 |
MSV3d | rs201348482 |
GWAS Ctlg | rs201348482 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201348482(A;A) |
Alt | rs201348482(A;A) |
Reference | Rs201348482(G;G) |
Significance | Pathogenic |
Disease | Hermansky-Pudlak syndrome 9 |
Variation | info |
Gene | BLOC1S6 |
CLNDBN | Hermansky-Pudlak syndrome 9 |
Reversed | 1 |
HGVS | NC_000015.9:g.45895305C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023365.4, |