RGD:11611605 Rat Genome Database

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Variant: RGD:11611605 -  Homo sapiens

RGD ID: 11611605
RS ID: rs139607688
ClinVar ID: CV307457
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC105375056  TREM2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 41,127,619
GRCh38 6 41,159,881
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
LRG_631t1:c.393C>T
LRG_631:g.8304C>T
NG_011561.1:g.8304C>T
NC_000006.12:g.41159881G>A
More... 		04/30/2022 synonymous variant likely benign|uncertain significance adolescent <1 / 1 000 000 none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TREM2
Accession:NM_018965
Location:EXON

Gene Symbol:TREM2
Accession:NM_001271821
Location:EXON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000397560 CLINVAR
  RCV002524478 CLINVAR
dbSNP (RS) rs139607688 CLINVAR
MedGen C3661900 CLINVAR
  C4748657 CLINVAR
NCBI Gene TREM2 CLINVAR
OMIM 605086 CLINVAR
  618193 CLINVAR