List of variants reported as uncertain significance for immune system disorder by Blueprint Genetics

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

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004409.5(DMPK):c.161-189T>C	rs752437441	0.00001
NM_005188.4(CBL):c.2519G>C (p.Cys840Ser)	rs376536789

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