List of variants in gene BRCA1 reported as likely benign for bone marrow disorder

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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: 22

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.-19-361C>T	rs141625477	0.00217
NM_007294.4(BRCA1):c.1137T>G (p.Ile379Met)	rs56128296	0.00158
NM_007294.4(BRCA1):c.3083G>A (p.Arg1028His)	rs80357459	0.00106
NM_007294.4(BRCA1):c.5277+78G>A	rs80358107	0.00099
NM_007294.4(BRCA1):c.4883T>C (p.Met1628Thr)	rs4986854	0.00098
NM_007294.4(BRCA1):c.1427A>G (p.His476Arg)	rs55720177	0.00066
NM_007294.4(BRCA1):c.3024G>A (p.Met1008Ile)	rs1800704	0.00065
NM_007294.4(BRCA1):c.2566T>C (p.Tyr856His)	rs80356892	0.00046
NM_007294.4(BRCA1):c.1036C>T (p.Pro346Ser)	rs80357015	0.00032
NM_007294.4(BRCA1):c.736T>G (p.Leu246Val)	rs28897675	0.00026
NM_007294.4(BRCA1):c.1486C>T (p.Arg496Cys)	rs28897676	0.00023
NM_007294.4(BRCA1):c.571G>A (p.Val191Ile)	rs80357090	0.00021
NM_007294.4(BRCA1):c.827C>G (p.Thr276Arg)	rs80357436	0.00019
NM_007294.4(BRCA1):c.199G>T (p.Asp67Tyr)	rs80357102	0.00005
NM_007294.4(BRCA1):c.-19-3A>G	rs273898669	0.00004
NM_007294.4(BRCA1):c.2286A>T (p.Arg762Ser)	rs273898682	0.00004
NM_007294.4(BRCA1):c.427G>A (p.Glu143Lys)	rs80356991	0.00004
NM_007294.4(BRCA1):c.824G>A (p.Gly275Asp)	rs397509327	0.00002
NM_007294.4(BRCA1):c.1843TCT[1] (p.Ser616del)	rs80358329
NM_007294.4(BRCA1):c.3075A>C (p.Thr1025=)	rs786201258
NM_007294.4(BRCA1):c.4185+11TG[5]	rs273900723
NM_007294.4(BRCA1):c.5406A>C (p.Thr1802=)	rs879255493

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