RS587777542 AP1S2

Health Risk Chr X:15845378
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pettigrew syndrome
Pettigrew syndrome
Other Variants in AP1S2
rs2519915767 rs1933972061 rs1934209113 rs2519929746 rs1934205000 rs2519929717 rs2519914292 rs2519914351 rs2519929432 rs1934288587
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