RS200055232 KRT6B

Health Risk Chr 12:52447336
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in KRT6B
rs60627726 rs267607473 rs267607472 rs1131691901 rs150021015 rs1592169234 rs764620689 rs750932643 rs146988096 rs202222264
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