List of variants in gene combination RAD51D, RAD51L3-RFFL reported by True Health Diagnostics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.698A>G (p.Glu233Gly)	rs28363284	0.01102
NM_002878.4(RAD51D):c.695G>A (p.Arg232Gln)	rs28363283	0.00457
NM_002878.4(RAD51D):c.666A>G (p.Glu222=)	rs114012742	0.00131
NM_002878.4(RAD51D):c.263+1588A>G	rs180869630	0.00123
NM_002878.4(RAD51D):c.263+1509C>T	rs201506572	0.00116
NM_002878.4(RAD51D):c.493C>T (p.Arg165Trp)	rs544654228	0.00004
NM_002878.4(RAD51D):c.900A>G (p.Arg300=)	rs370634278	0.00001
NM_002878.4(RAD51D):c.621G>A (p.Ser207=)	rs749859221

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