rs587776771(CT;CT)

common in clinvar

Is a	genotype
of	rs587776771
Gene	HNF1B
Chromosome	17
Position	37,744,839
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(CT;CT)	0	common in clinvar
(G;G)	0	common in clinvar
(I;I)	0	common genotype