RS1064793395 EFTUD2

Health Risk Chr 17:44886582
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in EFTUD2
rs387906877 rs387906878 rs879253725 rs879253726 rs387906879 rs879253727 rs397515431 rs879253728 rs794729651 rs797045551
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