RS797044857 GRHL3

Health Risk Chr 1:24354474
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in GRHL3
rs371889064 rs138381915 rs2148651821 rs1315515436 rs2522581753 rs2522582333 rs2522646617 rs2522608482 rs2522622618 rs200425622
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