RS869320716 SLFN14

Health Risk Chr 17:35557411
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Platelet-type bleeding disorder 20
Inborn genetic diseases
Platelet-type bleeding disorder 20
Inborn genetic diseases
Other Variants in SLFN14
rs869320714 rs869320715 rs757188030 rs753345092 rs192498365 rs150974695 rs2072671208 rs190500366 rs774339589 rs919934942
Ask Dr. Hemsworth about this variant