ClinVar Genomic variation as it relates to human health
NM_001001547.2(CD36):c.120+399TG[12]
Germline
Classification
(2)
Pathogenic; protective
no assertion criteria provided
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 | |||
CD36 | - | - |
GRCh38 GRCh37 |
232 | 255 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
protective (1) |
|
Feb 1, 2003 | RCV000014496.35 | |
Pathogenic (1) |
|
Feb 1, 2003 | RCV000014495.28 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 27, 2024