rs386833873(-;CT)
From SNPedia
| Carrier of a Finnish congenital nephrotic syndrome (NPHS1) mutation |
| Is a | genotype |
| of | rs386833873 |
| Gene | NPHS1, KIRREL2 |
| Chromosome | 19 |
| Position | 35,851,609 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (-;CT) | 3 | Carrier of a Finnish congenital nephrotic syndrome (NPHS1) mutation |
| (CT;CT) | 0 | common in clinvar |
Unaffected in absence of a second NPHS1 gene mutation
