rs748863662
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | 3 | Carrier of an autosomal recessive polycystic kidney disease mutation |
| (T;T) | 0 | common/normal |
| Make rs748863662(C;C) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 6 |
| Position | 51659724 |
| Gene | LOC105375087, PKHD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs748863662 |
| dbSNP (classic) | rs748863662 |
| ClinGen | rs748863662 |
| ebi | rs748863662 |
| HLI | rs748863662 |
| Exac | rs748863662 |
| Gnomad | rs748863662 |
| Varsome | rs748863662 |
| LitVar | rs748863662 |
| Map | rs748863662 |
| PheGenI | rs748863662 |
| Biobank | rs748863662 |
| 1000 genomes | rs748863662 |
| hgdp | rs748863662 |
| ensembl | rs748863662 |
| geneview | rs748863662 |
| scholar | rs748863662 |
| rs748863662 | |
| pharmgkb | rs748863662 |
| gwascentral | rs748863662 |
| openSNP | rs748863662 |
| 23andMe | rs748863662 |
| SNPshot | rs748863662 |
| SNPdbe | rs748863662 |
| MSV3d | rs748863662 |
| GWAS Ctlg | rs748863662 |
| Max Magnitude | 3 |
