RS797044877 PHKA2

Health Risk Chr X:18940029
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Glycogen storage disease IXa1
Glycogen storage disease IXd
Glycogen storage disease IXa1
Thyroid cancer
nonmedullary
1
Inborn genetic diseases
Glycogen storage disease IXa1
Glycogen storage disease IXd
Glycogen storage disease IXa1
Thyroid cancer
nonmedullary
1
Other Variants in PHKA2
rs137852285 rs137852286 rs587776731 rs137852287 rs137852288 rs587776732 rs137852293 rs137852289 rs137852290 rs137852291
Ask Dr. Hemsworth about this variant