RS74315302 CTSK

Health Risk Chr 1:150804203
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What This Variant Does
"[OMIM:?]
Associated Conditions
Pyknodysostosis
Inborn genetic diseases
Pyknodysostosis
Inborn genetic diseases
Other Variants in CTSK
rs74315301 rs74315303 rs74315304 rs74315305 rs74315306 rs29001685 rs868112062 rs142097792 rs201446793 rs375958814
Ask Dr. Hemsworth about this variant