ClinVar Miner

List of variants reported as likely benign for X-linked severe congenital neutropenia

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_000377.2(WAS):c.360+8A>G rs1557006508
NM_000377.2(WAS):c.897G>A (p.Gly299=) rs782793103

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