RS797044888 RAD54L

Health Risk Chr 1:46267600
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in RAD54L
rs121908688 rs121908689 rs121908690 rs374567435 rs139487723 rs150138364 rs1660658865 rs368491231 rs112896925 rs751010909
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