RS387907356 WNT1

Health Risk Chr 12:48981411
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What This Variant Does
"CLNSIG=5
Associated Conditions
Osteogenesis imperfecta type 15
Inborn genetic diseases
OSTEOPOROSIS
EARLY-ONSET
SUSCEPTIBILITY TO
Osteogenesis imperfecta type 15
Inborn genetic diseases
OSTEOPOROSIS
EARLY-ONSET
SUSCEPTIBILITY TO
Other Variants in WNT1
rs387907353 rs387907354 rs387907355 rs387907357 rs387907358 rs387907359 rs397514702 rs727505392 rs1555178899 rs769853984
Ask Dr. Hemsworth about this variant