List of variants reported as uncertain significance for Thrombocytopenia 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_014915.3(ANKRD26):c.153C>G (p.His51Gln)	rs139049098	0.00021
NM_014915.3(ANKRD26):c.4078A>G (p.Ile1360Val)	rs755787377	0.00004
NM_014915.3(ANKRD26):c.826C>T (p.Pro276Ser)	rs758179353	0.00004
NM_014915.3(ANKRD26):c.4271A>T (p.Asp1424Val)	rs560228865	0.00001
NM_014915.3(ANKRD26):c.1721ATG[7] (p.Asp579_Gly580insAsp)	rs561705414
NM_014915.3(ANKRD26):c.3765G>C (p.Glu1255Asp)
NM_014915.3(ANKRD26):c.5AGA[1] (p.Lys3del)
NM_014915.3(ANKRD26):c.789C>G (p.Asp263Glu)	rs777702991
NM_014915.3(ANKRD26):c.862T>C (p.Ser288Pro)

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