RGD:15176160 Rat Genome Database

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Variant: RGD:15176160 -  Homo sapiens

RGD ID: 15176160
RS ID: rs376904666
ClinVar ID: CV730280
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLIT2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 20,544,110
GRCh38 4 20,542,487
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001289136.3:c.2120-7G>A
NM_001289135.3:c.2132-7G>A
NM_004787.4:c.2144-7G>A
NG_047105.1:g.295563G>A
More... 		08/08/2017 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLIT2
Accession:NM_001289136
Location:INTRON

Gene Symbol:SLIT2
Accession:NM_001289135
Location:INTRON

Gene Symbol:SLIT2
Accession:XM_017008845
Location:INTRON

Gene Symbol:SLIT2
Accession:NM_004787
Location:INTRON

Gene Symbol:SLIT2
Accession:XM_006713986
Location:INTRON

Gene Symbol:SLIT2
Accession:XM_011513909
Location:INTRON

Gene Symbol:SLIT2
Accession:XM_005248211
Location:INTRON

Gene Symbol:SLIT2
Accession:XM_011513910
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000884524 CLINVAR
dbSNP (RS) rs376904666 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLIT2 CLINVAR
OMIM 603746 CLINVAR