List of variants reported as likely pathogenic for hematologic disorder by Undiagnosed Diseases Network, NIH

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001382567.1(STIM1):c.1681C>T (p.Arg561Cys)	rs142239530	0.00005
NM_002875.5(RAD51):c.772G>A (p.Glu258Lys)	rs1555429629

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