RS267606791 F8

Health Risk Chr X:154902150
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary factor VIII deficiency disease
Thyroid cancer
nonmedullary
1
Hereditary factor VIII deficiency disease
Thyroid cancer
nonmedullary
1
Other Variants in F8
rs137852354 rs137852355 rs137852356 rs137852357 rs137852358 rs137852359 rs137852360 rs28937294 rs28935499 rs137852361
Ask Dr. Hemsworth about this variant