RS142825013 FERMT1

Health Risk Chr 20:6079504
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Associated Conditions
Kindler syndrome
Inborn genetic diseases
Kindler syndrome
Inborn genetic diseases
Other Variants in FERMT1
rs1411462678 rs121918292 rs1568654138 rs1568664492 rs121918293 rs121918294 rs869312721 rs869312731 rs869312718 rs869312726
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