List of variants in gene BRCA1 reported as uncertain significance 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.2726A>T (p.Asn909Ile)	rs80357127	0.00003
NM_007294.4(BRCA1):c.441G>C (p.Leu147Phe)	rs748876625	0.00002
NM_007294.4(BRCA1):c.1922T>C (p.Ile641Thr)	rs730881474	0.00001
NM_007294.4(BRCA1):c.2597G>A (p.Arg866His)	rs80356911	0.00001
NM_007294.4(BRCA1):c.1043G>A (p.Cys348Tyr)	rs752198747
NM_007294.4(BRCA1):c.1983G>A (p.Arg661=)	rs869320788
NM_007294.4(BRCA1):c.4327C>G (p.Arg1443Gly)	rs41293455
NM_007294.4(BRCA1):c.4670A>G (p.Asp1557Gly)	rs869320779
NM_007294.4(BRCA1):c.5202T>G (p.Phe1734Leu)	rs869320780
NM_007294.4(BRCA1):c.5485G>A (p.Glu1829Lys)	rs869320789

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