rs369501114
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs369501114(A;A) |
Make rs369501114(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 71806186 |
Gene | CDH23 |
is a | snp |
is | mentioned by |
dbSNP | rs369501114 |
dbSNP (classic) | rs369501114 |
ClinGen | rs369501114 |
ebi | rs369501114 |
HLI | rs369501114 |
Exac | rs369501114 |
Gnomad | rs369501114 |
Varsome | rs369501114 |
LitVar | rs369501114 |
Map | rs369501114 |
PheGenI | rs369501114 |
Biobank | rs369501114 |
1000 genomes | rs369501114 |
hgdp | rs369501114 |
ensembl | rs369501114 |
geneview | rs369501114 |
scholar | rs369501114 |
rs369501114 | |
pharmgkb | rs369501114 |
gwascentral | rs369501114 |
openSNP | rs369501114 |
23andMe | rs369501114 |
SNPshot | rs369501114 |
SNPdbe | rs369501114 |
MSV3d | rs369501114 |
GWAS Ctlg | rs369501114 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369501114(A;A) |
Alt | rs369501114(A;A) |
Reference | Rs369501114(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CDH23 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.73565943G>A |
CLNSRC | |
CLNACC | RCV000485626.1, |