List of variants in gene combination LOC126805851, RBM8A reported as pathogenic for hematologic disorder

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005105.5(RBM8A):c.205+3_205+6del	rs1648185461
NM_005105.5(RBM8A):c.206-13C>A	rs1350809730
NM_005105.5(RBM8A):c.207_208insAGCG (p.Val70fs)	rs397515388

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