{{Rsnum
|rsid=4986763
|Gene=BRIP1
|Chromosome=17
|position=61683635
|Orientation=minus
|GMAF=0.332
|Gene_s=BRIP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 33.6 | 52.2 | 14.2
| HCB | 58.6 | 34.6 | 6.8
| JPT | 75.6 | 22.2 | 2.2
| YRI | 42.1 | 46.2 | 11.7
| ASW | 54.5 | 36.4 | 9.1
| CHB | 58.6 | 34.6 | 6.8
| CHD | 50.9 | 41.7 | 7.4
| GIH | 20.2 | 45.5 | 34.3
| LWK | 45.9 | 45.0 | 9.2
| MEX | 58.6 | 34.5 | 6.9
| MKK | 27.1 | 51.6 | 21.3
| TSI | 31.4 | 55.9 | 12.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=23473757
|Title=BRIP1 variations analysis reveals their relative importance as genetic susceptibility factor for cervical cancer
}}

{{PMID Auto
|PMID=19276285
|Title=Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.
|OA=1
}}

{{PMID Auto
|PMID=24301948
|Title=Further evidence for the contribution of the BRCA1-interacting protein-terminal helicase 1 (BRIP1) gene in breast cancer susceptibility
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}