List of variants reported as uncertain significance for combined immunodeficiency due to CRAC channel dysfunction by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_032790.4(ORAI1):c.1A>T (p.Met1Leu)	rs797044624	0.00004
NM_032790.4(ORAI1):c.140C>T (p.Pro47Leu)	rs781855511	0.00003
NM_001382567.1(STIM1):c.340C>T (p.Leu114Phe)	rs201767533	0.00001
NM_001382567.1(STIM1):c.605C>T (p.Pro202Leu)	rs1242032695	0.00001
NM_001382567.1(STIM1):c.1594C>A (p.Gln532Lys)	rs753214223
NM_001382567.1(STIM1):c.464G>A (p.Arg155Gln)	rs771484089

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