Annotation Detail
Information
- Associated Genes
- MS4A2
- Associated Variants
-
MS4A2 p.Glu237Gly (p.E237G)
(
ENST00000278888.8,
ENST00000617306.1 )
MS4A2 p.Glu237Gly (p.E237G) ( ENST00000278888.8, ENST00000617306.1 ) - Associated Disease
- RECLASSIFIED - POLYMORPHISM
- Source Database
- ClinVar
- Description
- NM_000139.5(MS4A2):c.710A>G (p.Glu237Gly) AND RECLASSIFIED - POLYMORPHISM
- ClinVar Allele ID
- 29846
- ClinVar RefSeq Alternation Syntax
- NM_001256916.2:c.575A>G
- ClinVar RefSeq Alternation Syntax
- NM_000139.5:c.710A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2001-09-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003333726
- ClinVar Disease
- RECLASSIFIED - POLYMORPHISM
- Observed Origin Sample
- germline
- Pubmed
- 8817330
- Pubmed
- 8842731
- Pubmed
- 11702205
Drugs