List of variants reported as uncertain significance for Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_138576.4(BCL11B):c.334C>G (p.Pro112Ala)	rs1477343612	0.00001
NM_138576.4(BCL11B):c.1219C>T (p.Pro407Ser)
NM_138576.4(BCL11B):c.1748C>T (p.Ala583Val)	rs769641126
NM_138576.4(BCL11B):c.182G>T (p.Cys61Phe)	rs2139953989

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