RS797044926 LAS1L

Health Risk Chr X:65523578
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in LAS1L
rs1173514495 rs1057518699 rs1057522039 rs200862250 rs867562406 rs1602612611 rs148048579 rs1410871672 rs752507559 rs769389600
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