RGD:156046803 Rat Genome Database

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Variant: RGD:156046803 -  Homo sapiens

RGD ID: 156046803
ClinVar ID: CV1978076
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DCHS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 6,652,109
GRCh38 11 6,630,878
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003737.4:c.3931-15C>T
NG_033858.2:g.29972C>T
NC_000011.10:g.6630878G>A
NC_000011.9:g.6652109G>A
 07/11/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DCHS1
Accession:NM_003737
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002590524 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DCHS1 CLINVAR
OMIM 603057 CLINVAR