List of variants in gene BRCA2 reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 47

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.7319A>G (p.His2440Arg)	rs4986860	0.00984
NM_000059.4(BRCA2):c.5199C>T (p.Ser1733=)	rs28897734	0.00488
NM_000059.4(BRCA2):c.6347A>G (p.His2116Arg)	rs55953736	0.00396
NM_000059.4(BRCA2):c.1275A>G (p.Glu425=)	rs34355306	0.00335
NM_000059.4(BRCA2):c.3869G>A (p.Cys1290Tyr)	rs41293485	0.00307
NM_000059.4(BRCA2):c.4068G>A (p.Leu1356=)	rs28897724	0.00295
NM_000059.4(BRCA2):c.68-7T>A	rs81002830	0.00277
NM_000059.4(BRCA2):c.6100C>T (p.Arg2034Cys)	rs1799954	0.00268
NM_000059.4(BRCA2):c.6323G>A (p.Arg2108His)	rs35029074	0.00260
NM_000059.4(BRCA2):c.8182G>A (p.Val2728Ile)	rs28897749	0.00239
NM_000059.4(BRCA2):c.3516G>A (p.Ser1172=)	rs1799952	0.00228
NM_000059.4(BRCA2):c.1792A>G (p.Thr598Ala)	rs28897710	0.00182
NM_000059.4(BRCA2):c.1798T>C (p.Tyr600His)	rs75419644	0.00170
NM_000059.4(BRCA2):c.125A>G (p.Tyr42Cys)	rs4987046	0.00158
NM_000059.4(BRCA2):c.8567A>C (p.Glu2856Ala)	rs11571747	0.00158
NM_000059.4(BRCA2):c.10110G>A (p.Arg3370=)	rs28897762	0.00132
NM_000059.4(BRCA2):c.8149G>T (p.Ala2717Ser)	rs28897747	0.00127
NM_000059.4(BRCA2):c.6821G>T (p.Gly2274Val)	rs55712212	0.00126
NM_000059.4(BRCA2):c.7504C>T (p.Arg2502Cys)	rs55716624	0.00100
NM_000059.4(BRCA2):c.1514T>C (p.Ile505Thr)	rs28897708	0.00074
NM_000059.4(BRCA2):c.4585G>A (p.Gly1529Arg)	rs28897728	0.00044
NM_000059.4(BRCA2):c.4584C>T (p.Ser1528=)	rs80359788	0.00026
NM_000059.4(BRCA2):c.9038C>T (p.Thr3013Ile)	rs28897755	0.00022
NM_000059.4(BRCA2):c.2350A>G (p.Met784Val)	rs11571653	0.00018
NM_000059.4(BRCA2):c.1889C>T (p.Thr630Ile)	rs80358479	0.00012
NM_000059.4(BRCA2):c.2538A>C (p.Ser846=)	rs11571654	0.00009
NM_000059.4(BRCA2):c.4977C>T (p.Ser1659=)	rs45484897	0.00009
NM_000059.4(BRCA2):c.7601C>T (p.Ala2534Val)	rs74047012	0.00009
NM_000059.4(BRCA2):c.6748A>G (p.Thr2250Ala)	rs80358899	0.00008
NM_000059.4(BRCA2):c.1662T>G (p.Cys554Trp)	rs80358451	0.00006
NM_000059.4(BRCA2):c.2320A>G (p.Thr774Ala)	rs55968715	0.00006
NM_000059.4(BRCA2):c.5268A>G (p.Val1756=)	rs199879914	0.00005
NM_000059.4(BRCA2):c.9087G>A (p.Ala3029=)	rs368576266	0.00005
NM_000059.4(BRCA2):c.6290C>T (p.Thr2097Met)	rs80358866	0.00004
NM_000059.4(BRCA2):c.9190G>A (p.Asp3064Asn)	rs80359177	0.00003
NM_000059.4(BRCA2):c.10154G>A (p.Arg3385His)	rs80358398	0.00002
NM_000059.4(BRCA2):c.2944A>C (p.Ile982Leu)	rs28897717	0.00002
NM_000059.4(BRCA2):c.5688A>G (p.Ala1896=)	rs768907899	0.00002
NM_000059.4(BRCA2):c.8014A>G (p.Ile2672Val)	rs80359037	0.00001
NM_000059.4(BRCA2):c.927A>G (p.Ser309=)	rs80359806	0.00001
NM_000059.4(BRCA2):c.1875T>A (p.Phe625Leu)	rs80358478
NM_000059.4(BRCA2):c.1909+9_1909+10del	rs527732001
NM_000059.4(BRCA2):c.3392G>A (p.Arg1131Lys)	rs1555283214
NM_000059.4(BRCA2):c.4090A>C (p.Ile1364Leu)	rs56248502
NM_000059.4(BRCA2):c.4563A>C (p.Leu1521=)	rs206075
NM_000059.4(BRCA2):c.7163C>T (p.Thr2388Ile)	rs1555286026
NM_000059.4(BRCA2):c.9606G>C (p.Pro3202=)	rs755890067

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