List of variants reported as benign for UBTF-related disorder

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_014233.4(UBTF):c.1086C>T (p.Leu362=)	rs2228196	0.05374
NM_014233.4(UBTF):c.1365G>A (p.Lys455=)
NM_014233.4(UBTF):c.1501C>T (p.Leu501=)
NM_014233.4(UBTF):c.1836G>A (p.Lys612=)
NM_014233.4(UBTF):c.540-9C>G

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