List of variants in gene combination LOC130061310, RAD51C reported as pathogenic for bone marrow disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NC_000017.11:g.(?_58692634)_(58692798_?)del
NM_058216.3(RAD51C):c.145+2T>G	rs1057517641

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