List of variants in gene combination BRCA1, LOC111589215 reported as likely benign for breast-ovarian cancer, familial, susceptibility to, 1

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.-192T>C	rs113323025	0.00510
NM_007294.4(BRCA1):c.-20+11C>T	rs273898672	0.00042
NM_007294.4(BRCA1):c.-20+57G>A	rs556032779	0.00002
NM_007294.4(BRCA1):c.-20+28G>A	rs904265019	0.00001
NM_007294.4(BRCA1):c.-20+55G>A	rs772215665	0.00001
NC_000017.11:g.43125443A>C	rs113323025
NM_007294.4(BRCA1):c.-20+521_-20+525del	rs770929332
NM_007294.4(BRCA1):c.-20+5T>C	rs1057524628
NM_007294.4(BRCA1):c.-53C>T	rs1597925819

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