RS797044922 PTCHD1

Health Risk Chr X:23393353
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in PTCHD1
rs727504113 rs150186077 rs150912089 rs369968343 rs878854360 rs879255587 rs878854361 rs147324438 rs138702144 rs139310513
Ask Dr. Hemsworth about this variant