List of variants in gene combination LOC126805851, RBM8A reported as benign 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005105.5(RBM8A):c.240C>T (p.Val80=)	rs1806851	0.00473
NM_005105.5(RBM8A):c.205+17C>A	rs115417561	0.00191
NM_005105.5(RBM8A):c.318C>T (p.Leu106=)	rs139097271	0.00086
NM_005105.5(RBM8A):c.206-13del
NM_005105.5(RBM8A):c.206-20T>C	rs117017431

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