List of variants in gene combination LOC129390903, RAD51C reported as likely pathogenic for hematologic 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.705+1G>A	rs876658644
NM_058216.3(RAD51C):c.705+1G>T	rs876658644
NM_058216.3(RAD51C):c.705G>T (p.Lys235Asn)	rs755849719

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