XRCC3, IVS5, A-G, -14

Variation ID: Help
8945
Review status: Help
(0/4) no assertion criteria provided0 stars out of maximum of 4 stars

Interpretation Help

Clinical significance:
risk factor
Last evaluated:
Jun 1, 2002
Number of submission(s):
1
Condition(s):
Breast cancer, susceptibility to[MedGen]
See supporting ClinVar records

Allele(s) Help

XRCC3, IVS5, A-G, -14

Allele ID:
23984
Variant type:
single nucleotide variant
Cytogenetic location:
14q32.3
Other names:
  • IVS5, A-G, -14
Links:
OMIM: 600675.0002

1 Affected gene

Variant frequency in dbGaP Help

No dbGaP data has been submitted for this variant.

Assertion and evidence details

Germline

Clinical significance
(Last evaluated)
Review status
(Assertion method)
Collection methodCondition(s)
(Mode of inheritance)
OriginCitationsSubmitter - Study nameSubmission accession
risk factor
(Jun 1, 2002)
no assertion criteria providedliterature only
  • Breast cancer, susceptibility to[MedGen]
germlineOMIMSCV000029719.2
SubmitterFamiliesIndividualsAllele originEthnicityGeographic originCitations and DatabasesDescription
OMIMnot providednot providedgermlinenot providednot providednot provided
SubmitterAllele originIndividualsPhenotypes (Affected status)EthnicityGeographic originCitationsDescription

Last Updated: Apr 12, 2017