rs76403709 Rat Genome Database

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Variant: rs76403709 -  Homo sapiens

RGD ID: 14726305
RS ID: rs76403709
ClinVar ID: CV660786
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GABRB2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 160,762,158
GRCh38 5 161,335,151
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000813.3:c.680-247C>T
NG_047050.1:g.217974C>T
NC_000005.10:g.161335151G>A
NC_000005.9:g.160762158G>A
More... 		06/14/2018 intron variant likely benign none provided

Gene Symbol:GABRB2
Accession:NM_000813
Location:INTRON

Gene Symbol:GABRB2
Accession:NM_021911
Location:INTRON

Gene Symbol:GABRB2
Accession:NM_001371727
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV000833812 CLINVAR
dbSNP (RS) rs76403709 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GABRB2 CLINVAR
OMIM 600232 CLINVAR