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

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.568G>A (p.Ala190Thr)	rs80116829	0.00167
NM_002878.4(RAD51D):c.146C>T (p.Ala49Val)	rs140317560	0.00116
NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn)	rs145309168	0.00041
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser)	rs140825795	0.00037
NM_002878.4(RAD51D):c.413A>G (p.Asn138Ser)	rs201676898	0.00025
NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile)	rs138969595	0.00021
NM_002878.4(RAD51D):c.904-3C>T	rs45478491	0.00018
NM_002878.4(RAD51D):c.137C>G (p.Ser46Cys)	rs587780102	0.00010
NM_002878.4(RAD51D):c.196G>A (p.Val66Met)	rs56026142	0.00009
NM_002878.4(RAD51D):c.394G>A (p.Val132Ile)	rs201141245	0.00007
NM_002878.4(RAD51D):c.629C>T (p.Ala210Val)	rs376855484	0.00006
NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp)	rs770250516	0.00006
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)	rs587781813	0.00004
NM_002878.4(RAD51D):c.53A>G (p.Gln18Arg)	rs546225564	0.00003
NM_002878.4(RAD51D):c.131G>A (p.Gly44Asp)	rs374730714	0.00001
NM_002878.4(RAD51D):c.286G>T (p.Gly96Cys)	rs762951311	0.00001
NM_002878.4(RAD51D):c.433C>T (p.Arg145Cys)	rs755173206	0.00001
NM_002878.4(RAD51D):c.716G>A (p.Arg239Gln)	rs780921112	0.00001
NM_002878.4(RAD51D):c.739-3C>T	rs1235042092	0.00001
NM_002878.4(RAD51D):c.339A>C (p.Lys113Asn)	rs786202507
NM_002878.4(RAD51D):c.349T>A (p.Cys117Ser)	rs786201358
NM_002878.4(RAD51D):c.785C>T (p.Pro262Leu)	rs730881950

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