Annotation Detail
Information
- Associated Genes
- MEFV
- Associated Variants
-
MEFV p.Arg42Trp (p.R42W)
(
ENST00000541159.5,
ENST00000339854.8,
ENST00000219596.6,
ENST00000536379.5 )
MEFV p.Arg42Trp (p.R42W) ( ENST00000219596.6, ENST00000339854.8, ENST00000536379.5, ENST00000541159.5 ) - Associated Disease
- familial Mediterranean fever
- Source Database
- ClinVar
- Description
- NM_000243.3(MEFV):c.124C>T (p.Arg42Trp) AND Familial Mediterranean fever
- ClinVar Allele ID
- 231956
- ClinVar RefSeq Alternation Syntax
- NM_000243.3:c.124C>T
- ClinVar RefSeq Alternation Syntax
- NM_001198536.2:c.124C>T
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2024-01-31
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000632798
- ClinVar Disease
- Familial Mediterranean fever
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs