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MIF, -173G-C

Variation ID: Help
14359
Review status: Help
(0/4) no assertion criteria provided0 stars out of maximum of 4 stars

Interpretation Help

Clinical significance:
risk factor
Last evaluated:
May 1, 2003
Number of submission(s):
1
Condition(s):
Rheumatoid arthritis, systemic juvenile, susceptibility to
See supporting ClinVar records

Allele(s) Help

MIF, -173G-C

Allele ID:
29398
Variant type:
single nucleotide variant
Cytogenetic location:
22q11.2
Other names:
  • -173G-C
Links:
OMIM: 153620.0001

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
(May 1, 2003)
no assertion criteria providedliterature only
  • Rheumatoid arthritis, systemic juvenile, susceptibility to
germlineOMIMSCV000035698.1
SubmitterFamiliesIndividualsAllele originEthnicityGeographic originCitations and DatabasesDescription
OMIMnot providednot providedgermlinenot providednot providednot provided
SubmitterAllele originIndividualsPhenotypes (Affected status)EthnicityGeographic originCitationsDescription

Last Updated: Dec 9, 2017