rs73797577 Rat Genome Database

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Variant: rs73797577 -  Homo sapiens

RGD ID: 14733611
RS ID: rs73797577
ClinVar ID: CV661184
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GABRB2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 160,762,029
GRCh38 5 161,335,022
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_021911.3:c.680-118G>T
NM_000813.3:c.680-118G>T
NG_047050.1:g.218103G>T
NC_000005.10:g.161335022C>A
More... 		06/14/2018 intron variant likely benign none provided

Gene Symbol:GABRB2
Accession:NM_001371727
Location:INTRON

Gene Symbol:GABRB2
Accession:NM_000813
Location:INTRON

Gene Symbol:GABRB2
Accession:NM_021911
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV000837173 CLINVAR
dbSNP (RS) rs73797577 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GABRB2 CLINVAR
OMIM 600232 CLINVAR