RS147622517 NEBL

Health Risk Chr 10:20888199
Upload your DNA to see your genotype for this variant.
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Primary dilated cardiomyopathy
Hypertrophic cardiomyopathy
Distal monosomy 10p
NEBL-related disorder
sudden unexplained death in epilepsy
Sudden unexplained death
Long QT syndrome
Primary familial hypertrophic cardiomyopathy
Primary dilated cardiomyopathy
Hypertrophic cardiomyopathy
Distal monosomy 10p
NEBL-related disorder
sudden unexplained death in epilepsy
Sudden unexplained death
Other Variants in NEBL
rs146275785 rs41277374 rs114875104 rs71578983 rs137973321 rs200705273 rs201822024 rs727504904 rs143644290 rs75301590
Ask Dr. Hemsworth about this variant