List of variants in gene BRIP1 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.206-2A>G	rs786203700	0.00001
NM_032043.3(BRIP1):c.2684_2687del (p.Val894_Ser895insTer)	rs760551339
NM_032043.3(BRIP1):c.2990_2993del (p.Thr997fs)	rs771028677
NM_032043.3(BRIP1):c.3353del (p.Asn1118fs)
NM_032043.3(BRIP1):c.507G>A (p.Gln169=)	rs876660937

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