rs386833873(CT;CT)

common in clinvar

Is a	genotype
of	rs386833873
Gene	NPHS1, KIRREL2
Chromosome	19
Position	35,851,609
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(-;CT)	3	Carrier of a Finnish congenital nephrotic syndrome (NPHS1) mutation
(CT;CT)	0	common in clinvar