List of variants in gene combination LOC130061310, RAD51C reported as likely 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: 18

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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+11C>G	rs1263551026	0.00001
NM_058216.3(RAD51C):c.145+13G>A	rs1177750681	0.00001
NM_058216.3(RAD51C):c.145+10C>A
NM_058216.3(RAD51C):c.145+10C>G
NM_058216.3(RAD51C):c.145+10C>T
NM_058216.3(RAD51C):c.145+11C>T
NM_058216.3(RAD51C):c.145+12T>C
NM_058216.3(RAD51C):c.145+13G>C	rs1177750681
NM_058216.3(RAD51C):c.145+14A>G	rs1567783355
NM_058216.3(RAD51C):c.145+15T>C	rs780116924
NM_058216.3(RAD51C):c.145+16G>A	rs1471520258
NM_058216.3(RAD51C):c.145+17G>A	rs369854656
NM_058216.3(RAD51C):c.145+17G>T	rs369854656
NM_058216.3(RAD51C):c.145+18C>A
NM_058216.3(RAD51C):c.145+19A>G
NM_058216.3(RAD51C):c.145+7_145+17del	rs2143681500
NM_058216.3(RAD51C):c.145+8C>T	rs1555592121

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