ClinVar Genomic variation as it relates to human health
NM_006887.5(ZFP36L2):c.986C>T (p.Ala329Val)
Germline
Classification
(1)
Benign
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 | |||
LOC129933607 | - | - | - | GRCh38 | - | 18 |
ZFP36L2 | - | - |
GRCh38 GRCh37 |
43 | 75 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
ZFP36L2-related disorder
|
Benign (1) |
|
Jan 8, 2020 | RCV003976651.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 27, 2024