RGD:14715611 Rat Genome Database

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Variant: RGD:14715611 -  Homo sapiens

RGD ID: 14715611
RS ID: rs4416547
ClinVar ID: CV660632
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WFS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 6,293,967
GRCh38 4 6,292,240
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001145853.1:c.712+243G>A
NM_006005.3:c.712+243G>A
NG_011700.1:g.27391G>A
NC_000004.12:g.6292240G>A
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WFS1
Accession:NM_001145853
Location:INTRON

Gene Symbol:WFS1
Accession:NM_006005
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000829450 CLINVAR
dbSNP (RS) rs4416547 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WFS1 CLINVAR
OMIM 606201 CLINVAR