rs727503350
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs727503350(G;T) |
Make rs727503350(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 16 |
Position | 21719192 |
Gene | OTOA |
is a | snp |
is | mentioned by |
dbSNP | rs727503350 |
dbSNP (classic) | rs727503350 |
ClinGen | rs727503350 |
ebi | rs727503350 |
HLI | rs727503350 |
Exac | rs727503350 |
Gnomad | rs727503350 |
Varsome | rs727503350 |
LitVar | rs727503350 |
Map | rs727503350 |
PheGenI | rs727503350 |
Biobank | rs727503350 |
1000 genomes | rs727503350 |
hgdp | rs727503350 |
ensembl | rs727503350 |
geneview | rs727503350 |
scholar | rs727503350 |
rs727503350 | |
pharmgkb | rs727503350 |
gwascentral | rs727503350 |
openSNP | rs727503350 |
23andMe | rs727503350 |
SNPshot | rs727503350 |
SNPdbe | rs727503350 |
MSV3d | rs727503350 |
GWAS Ctlg | rs727503350 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727503350(T;T) |
Alt | rs727503350(T;T) |
Reference | Rs727503350(G;G) |
Significance | Pathogenic |
Disease | Nonsyndromic hearing loss and deafness |
Variation | info |
Gene | OTOA |
CLNDBN | Nonsyndromic hearing loss and deafness |
Reversed | 0 |
HGVS | NC_000016.9:g.21730513G>T |
CLNSRC | |
CLNACC | RCV000151585.2, |