RS776191203 NBEAL2

Health Risk Chr 3:46995499
Upload your DNA to see your genotype for this variant.
Associated Conditions
Gray platelet syndrome
NBEAL2-related disorder
Inborn genetic diseases
Gray platelet syndrome
NBEAL2-related disorder
Inborn genetic diseases
Other Variants in NBEAL2
rs387907112 rs372277612 rs387907113 rs387907114 rs387907115 rs794726682 rs794726683 rs886041677 rs144664865 rs140354422
Ask Dr. Hemsworth about this variant