List of variants reported as uncertain significance for immune system disorder by Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001364905.1(LRBA):c.5030A>G (p.Asn1677Ser)	rs17027133	0.00349
NM_001364905.1(LRBA):c.1399A>G (p.Met467Val)	rs116355217	0.00225
NM_203447.4(DOCK8):c.3460C>T (p.Arg1154Cys)	rs34390308	0.00170
NM_003331.5(TYK2):c.648G>A (p.Pro216=)	rs142642403	0.00030
NM_003331.5(TYK2):c.1694G>A (p.Arg565Gln)	rs764267766	0.00001
NM_001290043.2(TAP2):c.629G>A (p.Arg210Gln)
NM_006912.6(RIT1):c.292A>T (p.Ile98Phe)
NM_022168.4(IFIH1):c.2200C>T (p.Leu734Phe)
NM_203447.4(DOCK8):c.3002T>C (p.Met1001Thr)	rs2054481229
NR_003051.4(RMRP):n.223G>T

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