List of variants in gene BRIP1 reported as pathogenic by Juno Genomics, Hangzhou Juno Genomics, Inc

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.2392C>T (p.Arg798Ter)	rs137852986	0.00010
NM_032043.3(BRIP1):c.1741C>T (p.Arg581Ter)	rs780020495	0.00002
NM_032043.3(BRIP1):c.189G>A (p.Trp63Ter)	rs1603367647
NM_032043.3(BRIP1):c.2244C>G (p.Tyr748Ter)	rs1257401983

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