RS587776913 FAM20A

Health Risk Chr 17:68540889
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What This Variant Does
"CLNSIG=5
Associated Conditions
Amelogenesis imperfecta type 1G
Amelogenesis imperfecta type 1G
Other Variants in FAM20A
rs144411158 rs587776911 rs587776912 rs587776914 rs387907215 rs587777530 rs139620139 rs587777531 rs1568724130 rs2086254952
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