ClinVar Miner

List of variants in gene WAS reported as likely pathogenic for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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NM_000377.2(WAS):c.257G>C (p.Arg86Pro) rs132630268
NM_000377.2(WAS):c.290G>A (p.Trp97Ter) rs1557006474
NM_000377.2(WAS):c.310C>T (p.Gln104Ter) rs193922414
NM_000377.2(WAS):c.553C>T (p.Gln185Ter) rs1557006672
NM_000377.2(WAS):c.763dup (p.Gln255fs) rs193922416
NM_000377.2(WAS):c.852del (p.Glu285fs) rs1557007035
NM_000377.3(WAS):c.397G>A (p.Glu133Lys)

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