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