rs797045088
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs797045088(A;A) |
Make rs797045088(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 133525153 |
Gene | EYA4, TARID |
is a | snp |
is | mentioned by |
dbSNP | rs797045088 |
dbSNP (classic) | rs797045088 |
ClinGen | rs797045088 |
ebi | rs797045088 |
HLI | rs797045088 |
Exac | rs797045088 |
Gnomad | rs797045088 |
Varsome | rs797045088 |
LitVar | rs797045088 |
Map | rs797045088 |
PheGenI | rs797045088 |
Biobank | rs797045088 |
1000 genomes | rs797045088 |
hgdp | rs797045088 |
ensembl | rs797045088 |
geneview | rs797045088 |
scholar | rs797045088 |
rs797045088 | |
pharmgkb | rs797045088 |
gwascentral | rs797045088 |
openSNP | rs797045088 |
23andMe | rs797045088 |
SNPshot | rs797045088 |
SNPdbe | rs797045088 |
MSV3d | rs797045088 |
GWAS Ctlg | rs797045088 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797045088(A;A) |
Alt | rs797045088(A;A) |
Reference | Rs797045088(G;G) |
Significance | Probable-Pathogenic |
Disease | Deafness |
Variation | info |
Gene | EYA4 TARID |
CLNDBN | Deafness, autosomal dominant 10 |
Reversed | 0 |
HGVS | NC_000006.11:g.133846291G>A |
CLNSRC | |
CLNACC | RCV000190582.1, |