rs369396703
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs369396703(A;A) |
Make rs369396703(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 71677444 |
Gene | CDH23 |
is a | snp |
is | mentioned by |
dbSNP | rs369396703 |
dbSNP (classic) | rs369396703 |
ClinGen | rs369396703 |
ebi | rs369396703 |
HLI | rs369396703 |
Exac | rs369396703 |
Gnomad | rs369396703 |
Varsome | rs369396703 |
LitVar | rs369396703 |
Map | rs369396703 |
PheGenI | rs369396703 |
Biobank | rs369396703 |
1000 genomes | rs369396703 |
hgdp | rs369396703 |
ensembl | rs369396703 |
geneview | rs369396703 |
scholar | rs369396703 |
rs369396703 | |
pharmgkb | rs369396703 |
gwascentral | rs369396703 |
openSNP | rs369396703 |
23andMe | rs369396703 |
SNPshot | rs369396703 |
SNPdbe | rs369396703 |
MSV3d | rs369396703 |
GWAS Ctlg | rs369396703 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369396703(A;A) |
Alt | rs369396703(A;A) |
Reference | Rs369396703(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | CDH23 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.73437201G>A |
CLNSRC | |
CLNACC | RCV000216452.1, RCV000486086.1, |