rs760574657
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs760574657(C;T) |
Make rs760574657(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 121168903 |
Gene | TECTA |
is a | snp |
is | mentioned by |
dbSNP | rs760574657 |
dbSNP (classic) | rs760574657 |
ClinGen | rs760574657 |
ebi | rs760574657 |
HLI | rs760574657 |
Exac | rs760574657 |
Gnomad | rs760574657 |
Varsome | rs760574657 |
LitVar | rs760574657 |
Map | rs760574657 |
PheGenI | rs760574657 |
Biobank | rs760574657 |
1000 genomes | rs760574657 |
hgdp | rs760574657 |
ensembl | rs760574657 |
geneview | rs760574657 |
scholar | rs760574657 |
rs760574657 | |
pharmgkb | rs760574657 |
gwascentral | rs760574657 |
openSNP | rs760574657 |
23andMe | rs760574657 |
SNPshot | rs760574657 |
SNPdbe | rs760574657 |
MSV3d | rs760574657 |
GWAS Ctlg | rs760574657 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs760574657(T;T) |
Alt | rs760574657(T;T) |
Reference | Rs760574657(C;C) |
Significance | Pathogenic |
Disease | Nonsyndromic hearing loss and deafness |
Variation | info |
Gene | TECTA |
CLNDBN | Nonsyndromic hearing loss and deafness |
Reversed | 0 |
HGVS | NC_000011.9:g.121039612C>T |
CLNSRC | |
CLNACC | RCV000220688.1, |