RS387907115 NBEAL2

Health Risk Chr 3:47004976
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Gray platelet syndrome
Gray platelet syndrome
Other Variants in NBEAL2
rs387907112 rs372277612 rs387907113 rs387907114 rs794726682 rs794726683 rs886041677 rs144664865 rs140354422 rs771754714
Ask Dr. Hemsworth about this variant