ClinVar Genomic variation as it relates to human health
NM_030662.4(MAP2K2):c.141C>T (p.Asp47=)
Germline
Top reviewed classifications are shown here.
Submission summary:
Reviewed by expert panel
Benign
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 | |||
MAP2K2 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
772 | 853 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (2) |
|
May 9, 2017 | RCV000523895.8 | |
Benign (1) |
|
Jun 17, 2021 | RCV001813495.3 | |
Benign (1) |
|
Jan 28, 2020 | RCV001637063.3 | |
Likely benign (1) |
|
May 13, 2021 | RCV002395242.2 |
Citations for germline classification of this variant
HelpText-mined citations for rs201526172 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated Sep 29, 2024