rs77626796 Rat Genome Database

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Variant: rs77626796 -  Homo sapiens

RGD ID: 150339711
RS ID: rs77626796
ClinVar ID: CV1167476
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GABBR2  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 101,052,561
GRCh38 9 98,290,279
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005458.8:c.*305A>C
NG_016426.1:g.423919A>C
NC_000009.12:g.98290279T>G
NC_000009.11:g.101052561T>G
 08/21/2019 3 prime utr variant benign none provided

Gene Symbol:GABBR2
Accession:NM_005458
Location:3UTRS;EXON

Gene Symbol:GABBR2
Accession:XM_005252316
Location:3UTRS;EXON

Gene Symbol:GABBR2
Accession:XM_017015331
Location:3UTRS;EXON

Gene Symbol:GABBR2
Accession:XM_017015332
Location:3UTRS;EXON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001534496 CLINVAR
dbSNP (RS) rs77626796 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GABBR2 CLINVAR
OMIM 607340 CLINVAR