rs201444177 Rat Genome Database

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Variant: rs201444177 -  Homo sapiens

RGD ID: 150500191
RS ID: rs201444177
ClinVar ID: CV1212164
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GABBR2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 101,133,717
GRCh38 9 98,371,435
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005458.8:c.1770+29T>C
NG_016426.1:g.342763T>C
NC_000009.12:g.98371435A>G
NC_000009.11:g.101133717A>G
 03/22/2021 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 RCV001594518 CLINVAR
dbSNP (RS) rs201444177 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GABBR2 CLINVAR
OMIM 607340 CLINVAR