rs150903392 Rat Genome Database

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Variant: rs150903392 -  Homo sapiens

RGD ID: 150428381
RS ID: rs150903392
ClinVar ID: CV1187530
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GABBR2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 101,150,999
GRCh38 9 98,388,717
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005458.8:c.1529+137G>A
NG_016426.1:g.325481G>A
NC_000009.12:g.98388717C>T
NC_000009.11:g.101150999C>T
 07/15/2018 intron variant likely benign none provided

Gene Symbol:GABBR2
Accession:XM_017015332
Location:INTRON

Gene Symbol:GABBR2
Accession:XM_017015331
Location:INTRON

Gene Symbol:GABBR2
Accession:XM_005252316
Location:INTRON

Gene Symbol:GABBR2
Accession:NM_005458
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001562192 CLINVAR
dbSNP (RS) rs150903392 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GABBR2 CLINVAR
OMIM 607340 CLINVAR