rs878853224
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs878853224(A;G) |
Make rs878853224(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 121187849 |
Gene | TECTA |
is a | snp |
is | mentioned by |
dbSNP | rs878853224 |
dbSNP (classic) | rs878853224 |
ClinGen | rs878853224 |
ebi | rs878853224 |
HLI | rs878853224 |
Exac | rs878853224 |
Gnomad | rs878853224 |
Varsome | rs878853224 |
LitVar | rs878853224 |
Map | rs878853224 |
PheGenI | rs878853224 |
Biobank | rs878853224 |
1000 genomes | rs878853224 |
hgdp | rs878853224 |
ensembl | rs878853224 |
geneview | rs878853224 |
scholar | rs878853224 |
rs878853224 | |
pharmgkb | rs878853224 |
gwascentral | rs878853224 |
openSNP | rs878853224 |
23andMe | rs878853224 |
SNPshot | rs878853224 |
SNPdbe | rs878853224 |
MSV3d | rs878853224 |
GWAS Ctlg | rs878853224 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853224(G;G) |
Alt | rs878853224(G;G) |
Reference | Rs878853224(A;A) |
Significance | Pathogenic |
Disease | Deafness |
Variation | info |
Gene | TECTA |
CLNDBN | Deafness, autosomal dominant 12 |
Reversed | 0 |
HGVS | NC_000011.9:g.121058558A>G |
CLNSRC | |
CLNACC | RCV000225015.1, |