List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.263+1588A>G	rs180869630	0.00123
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser)	rs140825795	0.00037
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=)	rs148690585	0.00028
NM_002878.4(RAD51D):c.904-3C>T	rs45478491	0.00018
NM_002878.4(RAD51D):c.145-4G>A	rs201361465	0.00006
NM_002878.4(RAD51D):c.621G>T (p.Ser207=)	rs749859221	0.00001
NM_002878.4(RAD51D):c.900A>G (p.Arg300=)	rs370634278	0.00001
NM_002878.4(RAD51D):c.231C>G (p.Thr77=)	rs376670250
NM_002878.4(RAD51D):c.263+1631C>T
NM_002878.4(RAD51D):c.294T>C (p.Tyr98=)
NM_002878.4(RAD51D):c.412A>C (p.Asn138His)	rs141690729
NM_002878.4(RAD51D):c.426A>G (p.Thr142=)	rs1597862600
NM_002878.4(RAD51D):c.708C>T (p.Thr236=)

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