rs372388344
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs372388344(A;A) |
| Make rs372388344(A;G) |
| Make rs372388344(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 71815099 |
| Gene | CDH23 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs372388344 |
| dbSNP (classic) | rs372388344 |
| ClinGen | rs372388344 |
| ebi | rs372388344 |
| HLI | rs372388344 |
| Exac | rs372388344 |
| Gnomad | rs372388344 |
| Varsome | rs372388344 |
| LitVar | rs372388344 |
| Map | rs372388344 |
| PheGenI | rs372388344 |
| Biobank | rs372388344 |
| 1000 genomes | rs372388344 |
| hgdp | rs372388344 |
| ensembl | rs372388344 |
| geneview | rs372388344 |
| scholar | rs372388344 |
| rs372388344 | |
| pharmgkb | rs372388344 |
| gwascentral | rs372388344 |
| openSNP | rs372388344 |
| 23andMe | rs372388344 |
| SNPshot | rs372388344 |
| SNPdbe | rs372388344 |
| MSV3d | rs372388344 |
| GWAS Ctlg | rs372388344 |
| Max Magnitude | 0 |
aka NM_022124.5(CDH23):c.9886G>A or (p.Asp3296Asn)
OMIM pathogenic variant
