List of variants reported as uncertain significance for Intellectual disability, X-linked, syndromic 33 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004606.5(TAF1):c.448A>G (p.Lys150Glu)	rs755220829	0.00001
NM_004606.5(TAF1):c.1436G>A (p.Gly479Glu)	rs2033907717
NM_004606.5(TAF1):c.1558G>C (p.Glu520Gln)	rs2520217569
NM_004606.5(TAF1):c.5315T>G (p.Met1772Arg)

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