RS140059558 MMP13

Health Risk Chr 11:102954174
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What This Variant Does
"CLNSIG=5
Associated Conditions
Metaphyseal chondrodysplasia
Spahr type
Metaphyseal anadysplasia 1
autosomal dominant
Metaphyseal chondrodysplasia
Spahr type
Metaphyseal anadysplasia 1
autosomal dominant
Other Variants in MMP13
rs121909497 rs121909498 rs121909499 rs121909500 rs369083541 rs17860530 rs374419716 rs797044754 rs886042854 rs150203792
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