rs2020912(C;T)

unclear if associated with hereditary nonpolyposis colorectal cancer (HNPCC5)

Is a	genotype
of	rs2020912
Gene	MSH6
Chromosome	2
Position	47,800,616
mentioned	by

Magnitude

2.5

Repute

Bad

Geno	Mag	Summary
(C;T)	2.5	unclear if associated with hereditary nonpolyposis colorectal cancer (HNPCC5)
(T;T)	0	common in clinvar

This variant is probably benign, but there is a possibility it is associated with hereditary nonpolyposis colorectal cancer type-5 (HNPCC5).