List of variants in gene BRIP1 reported as likely benign for Hereditary breast ovarian cancer syndrome

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.2098-22T>C	rs114505031	0.00684
NM_032043.3(BRIP1):c.206-21T>C	rs2048717	0.00589
NM_032043.3(BRIP1):c.1936-44C>A	rs139659736	0.00526
NM_032043.3(BRIP1):c.2493-50G>T	rs142108255	0.00191
NM_032043.3(BRIP1):c.1341-50G>T	rs150458297	0.00138
NM_032043.3(BRIP1):c.1255C>T (p.Arg419Trp)	rs150624408	0.00026
NM_032043.3(BRIP1):c.2380-23T>A	rs532683816	0.00023
NM_032043.3(BRIP1):c.3444C>A (p.Asp1148Glu)	rs28997573	0.00011
NM_032043.3(BRIP1):c.93+15G>A	rs113052745	0.00009
NM_032043.3(BRIP1):c.1140+11G>A	rs369153270	0.00006
NM_032043.3(BRIP1):c.1176A>G (p.Leu392=)	rs550092661	0.00006
NM_032043.3(BRIP1):c.1629-3T>C	rs587780828	0.00006
NM_032043.3(BRIP1):c.93+62C>T	rs921777989	0.00006
NM_032043.3(BRIP1):c.1340+64C>T	rs113218012	0.00001
NM_032043.3(BRIP1):c.1473+21G>A	rs113766686	0.00001
NM_032043.3(BRIP1):c.2257+25G>A	rs769919982	0.00001
NM_032043.3(BRIP1):c.1559G>C (p.Ser520Thr)	rs757629526
NM_032043.3(BRIP1):c.2258-21T>A	rs2077010216
NM_032043.3(BRIP1):c.380-28G>A	rs4988343

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