List of variants in gene combination LIX1L, LOC126805851, RBM8A reported as pathogenic, low penetrance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005105.5(RBM8A):c.-21G>A	rs139428292	0.01871
NM_005105.5(RBM8A):c.67+32G>C	rs201779890	0.00518

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