List of variants reported as likely pathogenic for immune system disorder by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.1065+1G>T	rs201089102
NM_002351.5(SH2D1A):c.385T>C (p.Ter129Arg)	rs111033625
NM_002351.5(SH2D1A):c.5A>G (p.Asp2Gly)	rs1556619319

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