RGD:150515904 Rat Genome Database

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Variant: RGD:150515904 -  Homo sapiens

RGD ID: 150515904
RS ID: rs9262289
ClinVar ID: CV1227706
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: VARS2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 30,885,686
GRCh38 6 30,917,909
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001167734.2:c.1075+103T>A
NM_001167733.3:c.565+103T>A
NM_020442.6:c.985+103T>A
NG_034224.1:g.8702T>A
More... 		06/23/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:VARS2
Accession:NM_020442
Location:INTRON

Gene Symbol:VARS2
Accession:NM_001167733
Location:INTRON

Gene Symbol:VARS2
Accession:NM_001167734
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001638981 CLINVAR
dbSNP (RS) rs9262289 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene VARS2 CLINVAR
OMIM 612802 CLINVAR