List of variants in gene BRCA1 reported as likely benign by Michigan Medical Genetics Laboratories, University of Michigan

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.594-34T>C	rs147314539	0.00010
NM_007294.4(BRCA1):c.1865C>T (p.Ala622Val)	rs56039126	0.00007
NM_007294.4(BRCA1):c.5278-14C>G	rs80358105	0.00006
NM_007294.4(BRCA1):c.425C>A (p.Pro142His)	rs55971303	0.00004
NM_007294.4(BRCA1):c.2447A>G (p.His816Arg)	rs80357108	0.00003
NM_007294.4(BRCA1):c.4097-11T>C	rs80358072	0.00002
NM_007294.4(BRCA1):c.522A>G (p.Gln174=)	rs765432756	0.00002
NM_007294.4(BRCA1):c.4358-45A>G	rs869320778	0.00001
NM_007294.4(BRCA1):c.-19-32AT[7]	rs273898667
NM_007294.4(BRCA1):c.1390A>G (p.Thr464Ala)	rs869320787

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