rs2808535 Rat Genome Database

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Variant: rs2808535 -  Homo sapiens

RGD ID: 150492704
RS ID: rs2808535
ClinVar ID: CV1238530
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GABBR2  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 101,340,070
GRCh38 9 98,577,788
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005458.8:c.459+147A>T
NG_016426.1:g.136410A>T
NC_000009.12:g.98577788T>A
NC_000009.11:g.101340070T>A
 07/15/2018 intron variant benign none provided

Gene Symbol:GABBR2
Accession:NM_005458
Location:INTRON

Gene Symbol:GABBR2
Accession:XM_005252316
Location:INTRON

Gene Symbol:GABBR2
Accession:XM_017015331
Location:INTRON

Gene Symbol:GABBR2
Accession:XM_017015332
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001655074 CLINVAR
dbSNP (RS) rs2808535 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GABBR2 CLINVAR
OMIM 607340 CLINVAR