rs137853042(C;C)

common in clinvar

Is a	genotype
of	rs137853042
Gene	NPHS1
Chromosome	19
Position	35,831,358
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Carrier of a congenital nephrotic syndrome mutation