List of variants reported as uncertain significance for thrombocytopenia 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000377.3(WAS):c.803G>A (p.Arg268Gln)	rs376560886	0.00009
NM_000377.3(WAS):c.1208C>T (p.Pro403Leu)	rs782666797	0.00006
NM_000377.3(WAS):c.1150C>T (p.Pro384Ser)	rs782761074	0.00004
NM_000377.3(WAS):c.463+3G>C	rs1274245256	0.00004
NM_000377.3(WAS):c.1388C>T (p.Ser463Leu)	rs782636781	0.00003
NM_000377.3(WAS):c.802C>T (p.Arg268Trp)	rs782149318	0.00002
NM_000377.3(WAS):c.975G>C (p.Gln325His)	rs930931192	0.00002
NM_000377.3(WAS):c.1156C>T (p.Pro386Ser)	rs895243178	0.00001
NM_000377.3(WAS):c.1219G>A (p.Gly407Arg)	rs782602857	0.00001
NM_000377.3(WAS):c.946C>A (p.Pro316Thr)	rs372779500	0.00001
NM_000377.3(WAS):c.962G>A (p.Arg321Gln)	rs782802310	0.00001
NM_000377.3(WAS):c.1203_1211dup (p.Pro402_Pro404dup)	rs2062430236
NM_000377.3(WAS):c.1391A>G (p.Glu464Gly)	rs2062432588
NM_000377.3(WAS):c.39_40delinsCC (p.Gly14Arg)	rs797044476

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