List of variants reported as uncertain significance for lymphatic system disorder by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.1686G>C (p.Gln562His)	rs77091385	0.00394
NM_002834.5(PTPN11):c.1658C>T (p.Thr553Met)	rs148176616	0.00048
NM_006939.4(SOS2):c.2600A>G (p.Asn867Ser)	rs561495878	0.00009
NM_005633.4(SOS1):c.1490G>A (p.Arg497Gln)	rs371314838	0.00004
NM_006939.4(SOS2):c.3547C>T (p.Pro1183Ser)	rs139401491	0.00002
NM_005633.4(SOS1):c.3290G>C (p.Ser1097Thr)	rs727505379	0.00001
NM_000081.4(LYST):c.655A>G (p.Met219Val)
NM_002834.5(PTPN11):c.1277A>C (p.His426Pro)	rs727505389
NM_005633.4(SOS1):c.3433G>A (p.Asp1145Asn)	rs727505383
NM_006912.6(RIT1):c.644_647del (p.Lys215fs)	rs766063111
NM_006939.4(SOS2):c.3013G>A (p.Asp1005Asn)
NM_006939.4(SOS2):c.775G>A (p.Gly259Ser)
NM_133459.4(CCBE1):c.700A>G (p.Thr234Ala)

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