rs267606619
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs267606619(C;T) |
Make rs267606619(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 1494 |
is a | snp |
is | mentioned by |
dbSNP | rs267606619 |
dbSNP (classic) | rs267606619 |
ClinGen | rs267606619 |
ebi | rs267606619 |
HLI | rs267606619 |
Exac | rs267606619 |
Gnomad | rs267606619 |
Varsome | rs267606619 |
LitVar | rs267606619 |
Map | rs267606619 |
PheGenI | rs267606619 |
Biobank | rs267606619 |
1000 genomes | rs267606619 |
hgdp | rs267606619 |
ensembl | rs267606619 |
geneview | rs267606619 |
scholar | rs267606619 |
rs267606619 | |
pharmgkb | rs267606619 |
gwascentral | rs267606619 |
openSNP | rs267606619 |
23andMe | rs267606619 |
SNPshot | rs267606619 |
SNPdbe | rs267606619 |
MSV3d | rs267606619 |
GWAS Ctlg | rs267606619 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267606619(T;T) |
Alt | rs267606619(T;T) |
Reference | Rs267606619(C;C) |
Significance | Drug-response |
Disease | Aminoglycoside-induced deafness Deafness aminoglycoside antibacterials response - Toxicity/ADR |
Variation | info |
Gene | |
CLNDBN | Aminoglycoside-induced deafness Deafness, nonsyndromic sensorineural, mitochondrial aminoglycoside antibacterials response - Toxicity/ADR |
Reversed | 0 |
HGVS | NC_012920.1:m.1494C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000010262.3, RCV000010263.3, RCV000211324.1, |