List of variants in gene combination RAD51D, RAD51L3-RFFL reported as uncertain significance by GeneKor MSA

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn)	rs145309168	0.00041
NM_002878.4(RAD51D):c.413A>G (p.Asn138Ser)	rs201676898	0.00025
NM_002878.4(RAD51D):c.394G>A (p.Val132Ile)	rs201141245	0.00007
NM_002878.4(RAD51D):c.493C>T (p.Arg165Trp)	rs544654228	0.00004
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)	rs587781813	0.00004
NM_002878.4(RAD51D):c.164G>A (p.Arg55Gln)	rs151198586	0.00002
NM_002878.4(RAD51D):c.784C>A (p.Pro262Thr)	rs1340405420	0.00001
NM_002878.4(RAD51D):c.270T>A (p.Asp90Glu)	rs1567728766
NM_002878.4(RAD51D):c.412A>C (p.Asn138His)	rs141690729
NM_002878.4(RAD51D):c.493C>G (p.Arg165Gly)	rs544654228
NM_002878.4(RAD51D):c.620C>G (p.Ser207Trp)	rs370228071
NM_002878.4(RAD51D):c.931A>G (p.Ile311Val)	rs755265519
NM_002878.4(RAD51D):c.933T>G (p.Ile311Met)	rs886052817

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