RS1064794916 PUF60

Health Risk Chr 8:143816706
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
8q24.3 microdeletion syndrome
Inborn genetic diseases
8q24.3 microdeletion syndrome
Other Variants in PUF60
rs398123001 rs886041995 rs1057518014 rs1057518046 rs1057518681 rs1064795388 rs1554641549 rs1085307134 rs1085307139 rs1085307138
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