List of variants in gene BARD1 reported by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1972C>T (p.Arg658Cys)	rs3738888	0.00736
NM_000465.4(BARD1):c.1738G>A (p.Glu580Lys)	rs35306212	0.00455
NM_000465.4(BARD1):c.1977A>G (p.Arg659=)	rs147215925	0.00230
NM_000465.4(BARD1):c.2282G>A (p.Ser761Asn)	rs142155101	0.00153
NM_000465.4(BARD1):c.144G>A (p.Leu48=)	rs151168457	0.00050
NM_000465.4(BARD1):c.1491A>G (p.Pro497=)	rs61754117	0.00027
NM_000465.4(BARD1):c.1694G>A (p.Arg565His)	rs146946984	0.00009
NM_000465.4(BARD1):c.1793C>A (p.Thr598Asn)	rs376256852	0.00006
NM_000465.4(BARD1):c.716T>A (p.Leu239Gln)	rs200359745	0.00006
NM_000465.4(BARD1):c.353A>G (p.Asn118Ser)	rs142864491	0.00004
NM_000465.4(BARD1):c.2071C>T (p.Leu691Phe)	rs1036838204	0.00001
NM_000465.4(BARD1):c.1070T>C (p.Ile357Thr)	rs587781555
NM_000465.4(BARD1):c.1071A>C (p.Ile357=)	rs786202366
NM_000465.4(BARD1):c.684A>T (p.Glu228Asp)	rs780627045

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