rs367928692
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs367928692(A;A) |
Make rs367928692(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 71791123 |
Gene | CDH23, MIR7152 |
is a | snp |
is | mentioned by |
dbSNP | rs367928692 |
dbSNP (classic) | rs367928692 |
ClinGen | rs367928692 |
ebi | rs367928692 |
HLI | rs367928692 |
Exac | rs367928692 |
Gnomad | rs367928692 |
Varsome | rs367928692 |
LitVar | rs367928692 |
Map | rs367928692 |
PheGenI | rs367928692 |
Biobank | rs367928692 |
1000 genomes | rs367928692 |
hgdp | rs367928692 |
ensembl | rs367928692 |
geneview | rs367928692 |
scholar | rs367928692 |
rs367928692 | |
pharmgkb | rs367928692 |
gwascentral | rs367928692 |
openSNP | rs367928692 |
23andMe | rs367928692 |
SNPshot | rs367928692 |
SNPdbe | rs367928692 |
MSV3d | rs367928692 |
GWAS Ctlg | rs367928692 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs367928692(A;A) |
Alt | rs367928692(A;A) |
Reference | Rs367928692(G;G) |
Significance | Pathogenic |
Disease | Usher syndrome not provided |
Variation | info |
Gene | MIR7152 CDH23 |
CLNDBN | Usher syndrome, type 1D not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.73550880G>A |
CLNSRC | ClinVar |
CLNACC | RCV000039236.3, RCV000239237.2, |