Annotation Detail
Information
- Associated Genes
- TREM2
- Associated Variants
-
TREM2 p.His157Tyr (p.H157Y)
(
ENST00000338469.3,
ENST00000373113.8,
ENST00000373122.8 )
TREM2 p.His157Tyr (p.H157Y) ( ENST00000338469.3, ENST00000373113.8, ENST00000373122.8 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_018965.4(TREM2):c.469C>T (p.His157Tyr) AND not specified
- ClinVar Allele ID
- 193655
- ClinVar RefSeq Alternation Syntax
- NM_001271821.2:c.469C>T
- ClinVar RefSeq Alternation Syntax
- NM_018965.4:c.469C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2015-05-11
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000177312
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs