List of variants reported as benign for X-linked lymphoproliferative disease due to SH2D1A deficiency by Illumina Laboratory Services, Illumina

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_002351.5(SH2D1A):c.*863T>A	rs7876065	0.84013
NC_000023.11:g.124346297C>T	rs12164382	0.43694
NM_002351.5(SH2D1A):c.*1321A>G	rs6649207	0.16862
NM_002351.5(SH2D1A):c.*212G>A	rs5958475	0.06359
NM_002351.5(SH2D1A):c.*866A>G	rs767771720	0.02353
NM_002351.5(SH2D1A):c.*1100C>A	rs141513491	0.00923
NM_002351.4(SH2D1A):c.-318G>C	rs146024883	0.00649
NM_002351.4(SH2D1A):c.-247G>A	rs190166840	0.00231
NM_002351.5(SH2D1A):c.-74T>A	rs142160401	0.00059
NM_002351.5(SH2D1A):c.*1689C>A	rs186082107	0.00031
NM_002351.5(SH2D1A):c.346+3A>G	rs199706936	0.00031
NM_002351.5(SH2D1A):c.*257A>T	rs556331824	0.00003
NM_002351.5(SH2D1A):c.48C>T (p.Gly16=)	rs72610640

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