rs886044667
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Chromosome | 16 |
Position | 21728372 |
Gene | OTOA |
is a | snp |
is | mentioned by |
dbSNP | rs886044667 |
dbSNP (classic) | rs886044667 |
ClinGen | rs886044667 |
ebi | rs886044667 |
HLI | rs886044667 |
Exac | rs886044667 |
Gnomad | rs886044667 |
Varsome | rs886044667 |
LitVar | rs886044667 |
Map | rs886044667 |
PheGenI | rs886044667 |
Biobank | rs886044667 |
1000 genomes | rs886044667 |
hgdp | rs886044667 |
ensembl | rs886044667 |
geneview | rs886044667 |
scholar | rs886044667 |
rs886044667 | |
pharmgkb | rs886044667 |
gwascentral | rs886044667 |
openSNP | rs886044667 |
23andMe | rs886044667 |
SNPshot | rs886044667 |
SNPdbe | rs886044667 |
MSV3d | rs886044667 |
GWAS Ctlg | rs886044667 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886044667(A;A) |
Alt | rs886044667(A;A) |
Reference | Rs886044667(C;C) |
Significance | Probable-Pathogenic |
Disease | Deafness |
Variation | info |
Gene | OTOA |
CLNDBN | Deafness, autosomal recessive 22 |
Reversed | 0 |
HGVS | NC_000016.9:g.21739693C>A |
CLNSRC | |
CLNACC | RCV000303562.1, |