RGD:13446303 Rat Genome Database

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Variant: RGD:13446303 -  Homo sapiens

RGD ID: 13446303
RS ID: rs1553203865
ClinVar ID: CV437819
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHRNB2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 154,540,590
GRCh38 1 154,568,114
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008027.1:g.5334G>C
NC_000001.11:g.154568114G>C
NC_000001.10:g.154540590G>C
NM_000748.3:c.64+6G>C
 06/30/2017 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:CHRNB2
Accession:NM_000748
Location:INTRON

Gene Symbol:CHRNB2
Accession:XM_017000180
Location:INTRON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000513543 CLINVAR
dbSNP (RS) rs1553203865 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CHRNB2 CLINVAR
OMIM 118507 CLINVAR