List of variants in gene combination LOC130061310, RAD51C reported as uncertain significance for immune system 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.145+12T>G	rs377297129	0.00024
NM_058216.3(RAD51C):c.145+5C>A	rs876660577	0.00001
NM_058216.3(RAD51C):c.145+5C>T	rs876660577	0.00001
NC_000017.10:g.(?_56769999)_(56774226_?)dup
NM_058216.3(RAD51C):c.145+18C>T	rs763292447
NM_058216.3(RAD51C):c.145+2_145+3insTT	rs1567783294
NM_058216.3(RAD51C):c.145+3A>G	rs536596205
NM_058216.3(RAD51C):c.145+4A>G	rs1598449822
NM_058216.3(RAD51C):c.145+4dup

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