ClinVar Miner

List of variants in gene HAX1 reported as likely benign for autosomal recessive severe congenital neutropenia

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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NM_006118.3(HAX1):c.514G>A (p.Val172Ile) rs141970914

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