RGD:14737105 Rat Genome Database

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Variant: RGD:14737105 -  Homo sapiens

RGD ID: 14737105
RS ID: rs79823873
ClinVar ID: CV657089
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHRNB2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 154,543,506
GRCh38 1 154,571,030
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000748.3:c.366-159A>G
NG_008027.1:g.8250A>G
NC_000001.11:g.154571030A>G
NC_000001.10:g.154543506A>G
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CHRNB2
Accession:XM_017000180
Location:5UTRS;INTRON

Gene Symbol:CHRNB2
Accession:NM_000748
Location:INTRON

Gene Symbol:CHRNB2
Accession:XR_001736952
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000838789 CLINVAR
dbSNP (RS) rs79823873 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CHRNB2 CLINVAR
OMIM 118507 CLINVAR