TNF, -863C-A

Variation ID: Help
12390
Review status: Help
(0/4) no assertion criteria provided0 stars out of maximum of 4 stars

Interpretation Help

Clinical significance:
protective
Last evaluated:
Aug 1, 2006
Number of submission(s):
1
Condition(s):
Alzheimer disease, protection against[MedGen]
See supporting ClinVar records

Allele(s) Help

TNF, -863C-A

Allele ID:
27429
Variant type:
single nucleotide variant
Cytogenetic location:
6p21.3
Other names:
  • -863C-A
Links:
OMIM: 191160.0006

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
protective
(Aug 1, 2006)
no assertion criteria providedliterature only
  • Alzheimer disease, protection against[MedGen]
germlineOMIMSCV000033445.2
SubmitterFamiliesIndividualsAllele originEthnicityGeographic originCitations and DatabasesDescription
OMIMnot providednot providedgermlinenot providednot providednot provided
SubmitterAllele originIndividualsPhenotypes (Affected status)EthnicityGeographic originCitationsDescription

Last Updated: Oct 5, 2016