List of variants in gene RBM10 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_005676.5(RBM10):c.1435+4del	rs1064795088
NM_005676.5(RBM10):c.2296C>T (p.Arg766Cys)	rs1935843757
NM_005676.5(RBM10):c.2537+1G>A	rs2147224076
NM_005676.5(RBM10):c.2537_2537+3del
NM_005676.5(RBM10):c.2668-2A>G	rs1556782770
NM_005676.5(RBM10):c.355_358del (p.Glu119fs)	rs1602556716

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