List of variants in gene BRCA2 reported as uncertain significance by MVZ Praenatalmedizin und Genetik Nuernberg

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.1129G>C (p.Glu377Gln)	rs876658625
NM_000059.4(BRCA2):c.474A>G (p.Ser158=)	rs886041101
NM_000059.4(BRCA2):c.9311A>G (p.Lys3104Arg)	rs956554593

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