List of variants reported as uncertain significance for hematologic disorder by Clinical Genomics Laboratory, Stanford Medicine

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg)	rs34557412	0.00403
NM_001364905.1(LRBA):c.2849G>T (p.Cys950Phe)	rs751947187	0.00002
NM_000135.4(FANCA):c.4188A>G (p.Ile1396Met)	rs1441175300	0.00001
NM_000135.4(FANCA):c.26C>T (p.Ser9Phe)	rs752776388

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