rs786202200(G;G)

common in clinvar

Is a	genotype
of	rs786202200
Gene	SDHC
Chromosome	1
Position	161,328,395
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	0	common genotype
(A;G)	6.2	Hereditary PGL/PCC Syndrome
(G;G)	0	common in clinvar
(G;T)	6.2	Hereditary PGL/PCC Syndrome