RS587777872 MCM9

Health Risk Chr 6:118924038
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
46
XX ovarian dysgenesis-short stature syndrome
Premature ovarian failure 1
Non-obstructive azoospermia
46
XX ovarian dysgenesis-short stature syndrome
Premature ovarian failure 1
Non-obstructive azoospermia
Other Variants in MCM9
rs587777871 rs1060505058 rs200408257 rs1380220881 rs2534754715 rs1460351219 rs144338608 rs772472098 rs774660544
Ask Dr. Hemsworth about this variant