RS587776769 TGFBR2

Health Risk Chr 3:30691490
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What This Variant Does
"CLNSIG=5
Associated Conditions
Colorectal cancer
hereditary nonpolyposis
type 6
Colorectal cancer
hereditary nonpolyposis
type 6
Other Variants in TGFBR2
rs121918714 rs121918715 rs28934568 rs104893807 rs104893809 rs104893812 rs104893813 rs104893814 rs104893815 rs104893810
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