List of variants in gene RBBP8 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_002894.3(RBBP8):c.1072del (p.His358fs)	rs754390284	0.00002
NM_002894.3(RBBP8):c.139C>T (p.Gln47Ter)	rs762396810	0.00001
NM_002894.3(RBBP8):c.2515C>T (p.Arg839Ter)	rs1064796899
NM_002894.3(RBBP8):c.367G>T (p.Glu123Ter)	rs370650618

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