RS144567652 FANCM

Health Risk Chr 14:45198718
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs144567652, also known as c.5791C&gt
Associated Conditions
Fanconi anemia
Spermatogenic failure 28
Malignant germ cell tumor of ovary
Familial cancer of breast
Azoospermia
Hereditary nonpolyposis colorectal carcinoma
Premature ovarian failure 15
Fanconi anemia
Spermatogenic failure 28
Malignant germ cell tumor of ovary
Familial cancer of breast
Azoospermia
Hereditary nonpolyposis colorectal carcinoma
Premature ovarian failure 15
Other Variants in FANCM
rs797045116 rs151071546 rs61744648 rs143662421 rs112326758 rs142007602 rs77374493 rs202171930 rs200360968 rs146897650
Ask Dr. Hemsworth about this variant