ClinVar Miner

List of variants in gene NBEAL2 reported as pathogenic for Abnormal bleeding; Thrombocytopenia

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_015175.3(NBEAL2):c.6801+1G>C rs1285731171

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