List of variants in gene LOC129390903, LOC130061311, RAD51C studied for anemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NC_000017.11:g.(?_58703186)_(58734232_?)del
NC_000017.11:g.(?_58703196)_(58709990_?)del
NM_058216.1(RAD51C):c.572-?_(*1_?)del
NM_058216.2(RAD51C):c.572-?_*120del

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