List of variants in gene PHF21A reported as likely pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001352027.3(PHF21A):c.361-2A>C	rs2136081849	0.00001
NM_001352027.3(PHF21A):c.1227+1G>T	rs2496660796
NM_001352027.3(PHF21A):c.1684+2T>A	rs2495688598
NM_001352027.3(PHF21A):c.1741C>T (p.Arg581Ter)	rs1565138763

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