List of variants in gene SMARCD2 reported as likely pathogenic for immune system disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001098426.2(SMARCD2):c.391C>T (p.Gln131Ter)
NM_001098426.2(SMARCD2):c.568-1G>C	rs112986541
NM_001098426.2(SMARCD2):c.574C>T (p.Arg192Ter)	rs758123382
NM_001098426.2(SMARCD2):c.654del (p.Gly220fs)	rs2144630306

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