RS63750833 MSH6

Health Risk Chr 2:47801136
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What This Variant Does
"c.3155_3156delAG (p.Glu1052Valfs) 23andMe name: i5037890
Associated Conditions
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Hereditary nonpolyposis colon cancer
Endometrial carcinoma
Lynch syndrome 5
Inherited MMR deficiency (Lynch syndrome)
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Hereditary nonpolyposis colon cancer
Endometrial carcinoma
Lynch syndrome 5
Inherited MMR deficiency (Lynch syndrome)
Other Variants in MSH6
rs63750955 rs63751234 rs587776706 rs193922343 rs41294988 rs193922345 rs201892477 rs3136334 rs149945495 rs397515875
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