rs762705295
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs762705295(-;-) |
| Make rs762705295(-;A) |
| Make rs762705295(A;A) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 77012033 |
| Gene | KCNMA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs762705295 |
| dbSNP (classic) | rs762705295 |
| ClinGen | rs762705295 |
| ebi | rs762705295 |
| HLI | rs762705295 |
| Exac | rs762705295 |
| Gnomad | rs762705295 |
| Varsome | rs762705295 |
| LitVar | rs762705295 |
| Map | rs762705295 |
| PheGenI | rs762705295 |
| Biobank | rs762705295 |
| 1000 genomes | rs762705295 |
| hgdp | rs762705295 |
| ensembl | rs762705295 |
| geneview | rs762705295 |
| scholar | rs762705295 |
| rs762705295 | |
| pharmgkb | rs762705295 |
| gwascentral | rs762705295 |
| openSNP | rs762705295 |
| 23andMe | rs762705295 |
| SNPshot | rs762705295 |
| SNPdbe | rs762705295 |
| MSV3d | rs762705295 |
| GWAS Ctlg | rs762705295 |
| Max Magnitude | 0 |
aka NM_001014797.2(KCNMA1):c.2038dup or (p.Tyr680Leufs)
OMIM pathogenic variant
