XRCC3, IVS5, A-G, -14

XRCC3, IVS5, A-G, -14

Variant type:
single nucleotide variant
Cytogenetic location:
Other names:
  • IVS5, A-G, -14
OMIM: 600675.0002

Clinical significance

XRCC3, IVS5, A-G, -14

Clinical significance:
risk factor
Review status:
(0/4)0 stars out of maximum of 4 stars
no assertion criteria provided
Number of submission(s):
  • Breast cancer, susceptibility to[MedGen]
See supporting ClinVar records

Variant frequency in dbGaP (Help)

no data available

1 Affected gene

Assertion and evidence details


Clinical significance
(Last evaluated)
Review status
(Assertion method)
Collection methodCondition(s)
(Mode of inheritance)
OriginCitationsSubmitter - Study name
(Last submitted)
Submission accession
risk factor
(May 12, 2011)
no assertion criteria providedliterature only
  • Breast cancer, susceptibility to[MedGen]
germlinePubMed (1)
[See all records that cite this PMID]

(Dec 30, 2010)

SubmitterFamiliesIndividualsAllele originEthnicityGeographic originCitations and DatabasesDescription
OMIMnot providednot providedgermlinenot providednot providedPubMednot provided
SubmitterAllele originIndividualsPhenotypes (Affected status)EthnicityGeographic originCitationsDescription
OMIMgermlinenot providedBreast cancer, susceptibility to (not provided)not providednot providedPubMedKuschel et al. (2002) performed genetic association studies in a population-based breast cancer (see 114480) case-control study analyzing polymorphis…Full description

Last Updated: Sep 17, 2015