ClinVar Genomic variation as it relates to human health
NM_002415.2(MIF):c.221G>T (p.Arg74Leu)
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
MIF | - | - |
GRCh38 GRCh38 GRCh37 |
- | 136 | |
MIF-AS1 | - | - | - |
GRCh38 GRCh38 |
- | 58 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 3, 2023 | RCV004318629.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jul 29, 2024