List of variants reported as likely pathogenic for hematologic disorder by UCLA Clinical Genomics Center, UCLA

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg)	rs34557412	0.00403
NM_000402.4(G6PD):c.653C>T (p.Ser218Phe)	rs5030868	0.00028
NM_000132.4(F8):c.3169G>A (p.Glu1057Lys)	rs28933673	0.00014
NM_018389.5(SLC35C1):c.872C>T (p.Thr291Ile)	rs751828447	0.00001
NM_032638.5(GATA2):c.1113C>A (p.Asn371Lys)	rs376003468

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