RGD:11649732 Rat Genome Database

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Variant: RGD:11649732 -  Homo sapiens

RGD ID: 11649732
RS ID: rs886059533
ClinVar ID: CV299081
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WFS1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 6,304,453
GRCh38 4 6,302,726
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006005.3:c.*258A>G
NG_011700.1:g.37877A>G
NC_000004.12:g.6302726A>G
NC_000004.11:g.6304453A>G
More... 		06/14/2016 3 prime utr variant likely benign|uncertain significance Autosomal dominant nonsyndromic deafness 6; DEAFNESS, AUTOSOMAL DOMINANT 14; DEAFNESS, AUTOSOMAL DOMINANT 38; DEAFNESS, AUTOSOMAL DOMINANT 6; DFNA6/14/38 Nonsyndromic Low-Frequency Sensorineural Hearing Loss; WFS1-Related Disorders; WFS1-Related Low-Frequency Sensory Hearing Loss
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:WFS1
Accession:NM_006005
Location:3UTRS;EXON

Gene Symbol:WFS1
Accession:NM_001145853
Location:3UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:12955714   PMID:17603484   PMID:18060660   PMID:20301750   PMID:20738327   PMID:33879153  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000288853 CLINVAR
  RCV000346119 CLINVAR
  RCV003126698 CLINVAR
dbSNP (RS) rs886059533 CLINVAR
MedGen C1833021 CLINVAR
  C4551693 CLINVAR
  CN239410 CLINVAR
NCBI Gene WFS1 CLINVAR
OMIM 222300 CLINVAR
  600965 CLINVAR
  606201 CLINVAR