rs267607107
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs267607107(A;A) |
Make rs267607107(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 121166665 |
Gene | TECTA |
is a | snp |
is | mentioned by |
dbSNP | rs267607107 |
dbSNP (classic) | rs267607107 |
ClinGen | rs267607107 |
ebi | rs267607107 |
HLI | rs267607107 |
Exac | rs267607107 |
Gnomad | rs267607107 |
Varsome | rs267607107 |
LitVar | rs267607107 |
Map | rs267607107 |
PheGenI | rs267607107 |
Biobank | rs267607107 |
1000 genomes | rs267607107 |
hgdp | rs267607107 |
ensembl | rs267607107 |
geneview | rs267607107 |
scholar | rs267607107 |
rs267607107 | |
pharmgkb | rs267607107 |
gwascentral | rs267607107 |
openSNP | rs267607107 |
23andMe | rs267607107 |
SNPshot | rs267607107 |
SNPdbe | rs267607107 |
MSV3d | rs267607107 |
GWAS Ctlg | rs267607107 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267607107(A;A) |
Alt | rs267607107(A;A) |
Reference | Rs267607107(G;G) |
Significance | Pathogenic |
Disease | Deafness |
Variation | info |
Gene | TECTA |
CLNDBN | Deafness, autosomal dominant 12 |
Reversed | 0 |
HGVS | NC_000011.9:g.121037374G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000007428.2, |