Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204707(A;G)

From SNPedia

(Redirected from I6016828(C;T))

Jump to:navigation, search

Carrier of an autosomal recessive polycystic kidney disease mutation

Is a	genotype
of	rs786204707
Gene	PKHD1
Chromosome	6
Position	52,043,636
mentioned	by

3

Bad

Geno	Mag	Summary
(A;G)	3	Carrier of an autosomal recessive polycystic kidney disease mutation
(G;G)	0	common in clinvar

Retrieved from "https://www.SNPedia.com/index.php?title=Rs786204707(A;G)&oldid=1201951"

Is a genotype