rs397515585
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs397515585(-;-) |
Make rs397515585(-;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 26480980 |
Gene | OTOF |
is a | snp |
is | mentioned by |
dbSNP | rs397515585 |
dbSNP (classic) | rs397515585 |
ClinGen | rs397515585 |
ebi | rs397515585 |
HLI | rs397515585 |
Exac | rs397515585 |
Gnomad | rs397515585 |
Varsome | rs397515585 |
LitVar | rs397515585 |
Map | rs397515585 |
PheGenI | rs397515585 |
Biobank | rs397515585 |
1000 genomes | rs397515585 |
hgdp | rs397515585 |
ensembl | rs397515585 |
geneview | rs397515585 |
scholar | rs397515585 |
rs397515585 | |
pharmgkb | rs397515585 |
gwascentral | rs397515585 |
openSNP | rs397515585 |
23andMe | rs397515585 |
SNPshot | rs397515585 |
SNPdbe | rs397515585 |
MSV3d | rs397515585 |
GWAS Ctlg | rs397515585 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397515585(-;-) |
Alt | rs397515585(-;-) |
Reference | Rs397515585(G;G) |
Significance | Pathogenic |
Disease | Deafness |
Variation | info |
Gene | OTOF |
CLNDBN | Deafness, autosomal recessive 9 |
Reversed | 1 |
HGVS | NC_000002.11:g.26703848delC |
CLNSRC | ClinVar GeneReviews |
CLNACC | RCV000056019.1, |