rs202052174
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs202052174(A;A) |
Make rs202052174(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 71803371 |
Gene | CDH23 |
is a | snp |
is | mentioned by |
dbSNP | rs202052174 |
dbSNP (classic) | rs202052174 |
ClinGen | rs202052174 |
ebi | rs202052174 |
HLI | rs202052174 |
Exac | rs202052174 |
Gnomad | rs202052174 |
Varsome | rs202052174 |
LitVar | rs202052174 |
Map | rs202052174 |
PheGenI | rs202052174 |
Biobank | rs202052174 |
1000 genomes | rs202052174 |
hgdp | rs202052174 |
ensembl | rs202052174 |
geneview | rs202052174 |
scholar | rs202052174 |
rs202052174 | |
pharmgkb | rs202052174 |
gwascentral | rs202052174 |
openSNP | rs202052174 |
23andMe | rs202052174 |
SNPshot | rs202052174 |
SNPdbe | rs202052174 |
MSV3d | rs202052174 |
GWAS Ctlg | rs202052174 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs202052174(A;A) |
Alt | rs202052174(A;A) |
Reference | Rs202052174(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | CDH23 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000010.10:g.73563128G>A |
CLNSRC | ClinVar |
CLNACC | RCV000039276.4, |