RS200622688 NBEAL2

Health Risk Chr 3:47002158
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Associated Conditions
Gray platelet syndrome
Thrombocytopenia
Abnormal bleeding
Inborn genetic diseases
Gray platelet syndrome
Thrombocytopenia
Abnormal bleeding
Inborn genetic diseases
Other Variants in NBEAL2
rs387907112 rs372277612 rs387907113 rs387907114 rs387907115 rs794726682 rs794726683 rs886041677 rs144664865 rs140354422
Ask Dr. Hemsworth about this variant