RS1064794967 HNRNPK

Health Risk Chr 9:83975471
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in HNRNPK
rs863223402 rs863223403 rs879255263 rs886041807 rs767454980 rs960183341 rs1085307831 rs1554698658 rs1554699378 rs1554700678
Ask Dr. Hemsworth about this variant