{{Rsnum
|rsid=2229571
|Gene=BARD1
|Chromosome=2
|position=214780740
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.4876
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=BARD1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 33.8 | 47.7 | 18.5
| HCB | 13.3 | 42.2 | 44.4
| JPT | 6.8 | 47.7 | 45.5
| YRI | 19.0 | 41.3 | 39.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 13.3 | 42.2 | 44.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=2229571
|allele=G
|frequency=0.417
|uid=1103658361181
|type=heterozygous_SNP
|hugo=BARD1
|ensembl gene=ENSG00000138376
|ensembl transcript=ENST00000260947
|sift=AFFECT FUNCTION
|disease=Defects in BARD1 gene are found in primary breast, ovarian and uterine cancers.
}}

{{PMID Auto
|PMID=19412175
|Title=Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.
|OA=1
}}

{{PMID Auto
|PMID=19482343
|Title=Polymorphisms in HPV E6/E7 protein interacted genes and risk of cervical cancer in Chinese women: a case-control analysis.
}}

{{GET Evidence
|gene=BARD1
|aa_change=Arg378Ser
|aa_change_short=R378S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2229571
|overall_frequency_n=5674
|overall_frequency_d=10758
|overall_frequency=0.527421
|n_genomes=41
|n_genomes_annotated=0
|n_haplomes=57
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.002
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}