RS587779344 PMS2

Health Risk Chr 7:5997349
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What This Variant Does
"rs587779344, also known as c.780delC or p.Asp261Metfs, represents a very rare mutation in the PMS2 g...
Associated Conditions
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Other Variants in PMS2
rs63750871 rs587776715 rs63751466 rs63750049 rs63750451 rs1057515571 rs1057515572 rs121434629 rs121434630 rs63750685
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