List of variants in gene BRCA2 reported as uncertain significance for Familial prostate cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.2459A>G (p.Asp820Gly)	rs80358511	0.00002
NM_000059.4(BRCA2):c.353G>A (p.Arg118His)	rs80358603	0.00002
NM_000059.4(BRCA2):c.215A>G (p.Asn72Ser)	rs276174818	0.00001
NM_000059.4(BRCA2):c.2918C>T (p.Ser973Leu)	rs397507296	0.00001
NM_000059.4(BRCA2):c.6287C>G (p.Pro2096Arg)	rs587781396	0.00001
NM_000059.4(BRCA2):c.6877T>C (p.Phe2293Leu)	rs80358912	0.00001
NM_000059.4(BRCA2):c.8183T>C (p.Val2728Ala)	rs587781719	0.00001
NM_000059.4(BRCA2):c.8432A>G (p.Asp2811Gly)	rs80359090	0.00001
NM_000059.4(BRCA2):c.847A>G (p.Ile283Val)	rs80359097	0.00001
NM_000059.4(BRCA2):c.9304G>A (p.Ala3102Thr)	rs747073940	0.00001
NM_000059.4(BRCA2):c.9863C>T (p.Thr3288Ile)	rs754588394	0.00001
NM_000059.4(BRCA2):c.2097G>T (p.Gln699His)	rs80358486
NM_000059.4(BRCA2):c.4031A>G (p.Asn1344Ser)	rs1593901214
NM_000059.4(BRCA2):c.41T>A (p.Ile14Asn)	rs1241704385
NM_000059.4(BRCA2):c.4641T>A (p.Asp1547Glu)	rs2137508622
NM_000059.4(BRCA2):c.476-10T>A	rs1593886998
NM_000059.4(BRCA2):c.5212A>G (p.Thr1738Ala)
NM_000059.4(BRCA2):c.5995G>A (p.Val1999Met)
NM_000059.4(BRCA2):c.6764C>T (p.Thr2255Ile)	rs2137530514
NM_000059.4(BRCA2):c.8152A>G (p.Ile2718Val)	rs2072757385
NM_000059.4(BRCA2):c.8744C>T (p.Ala2915Val)	rs1310128359
NM_000059.4(BRCA2):c.9015A>G (p.Arg3005=)	rs1060502477
NM_000059.4(BRCA2):c.9344A>G (p.Lys3115Arg)	rs276174923
NM_000059.4(BRCA2):c.9757T>C (p.Cys3253Arg)

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