RS797044906 FN1

Health Risk Chr 2:215404591
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in FN1
rs137854486 rs137854487 rs137854488 rs869025198 rs869025199 rs1064795155 rs1553658926 rs1553659131 rs1181638652 rs1553667072
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