NFKBIL1, -62T-A

NFKBIL1, -62T-A

Variant type:
single nucleotide variant
Cytogenetic location:
6p21.3
Other names:
  • -62T-A
Links:
OMIM: 601022.0001

Clinical significance

NFKBIL1, -62T-A

Clinical significance:
risk factor
Review status:
1 star out of maximum of 4 stars
classified by single submitter
Number of submission(s):
1
Condition(s)
See supporting ClinVar records

1 Affected Gene

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Assertion and evidence details

Germline

Clinical significance
(Last evaluated)
Review status
(Assertion method)
Collection methodCondition(s)
(Mode of inheritance)
OriginCitationsSubmitter
(Last submitted)
Submission accession
risk factor
(Jun 26, 2009)
classified by single submitter
(literature only)
literature onlygermlinePubMed (1)
OMIM
(Dec 30, 2010)
SCV000029210

Summary

FamiliesIndividualsSegregationAllele originEthnicityGeographic origin
not providednot providednot providedgermlinenot providednot provided

OMIM

Data published from literature

FamiliesIndividualsSegregationsAllele originCitations
not providednot providednot providedgermline

Description

Okamoto et al. (2003) identified a non-HLA-DRB1 (142857) major histocompatibility complex-linked susceptibility allele for rheumatoid arthritis (180300): the T allele of the -62T/A SNP of the NFKBIL1 gene.

Last Updated: Oct 30, 2014

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