List of variants in gene BRIP1 reported as pathogenic by Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego

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.1871C>A (p.Ser624Ter)	rs587781321	0.00006
NM_032043.3(BRIP1):c.1234_1235del (p.Glu412fs)	rs1064795649
NM_032043.3(BRIP1):c.2992_2993del (p.Lys998fs)	rs878855151
NM_032043.3(BRIP1):c.46del (p.Tyr16fs)	rs876660613

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