RGD:156386546 Rat Genome Database

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Variant: RGD:156386546 -  Homo sapiens

RGD ID: 156386546
ClinVar ID: CV1979798
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DCHS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 6,647,395
GRCh38 11 6,626,164
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000011.9:g.6647395C>T
NM_003737.4:c.6576+5G>A
NG_033858.2:g.34686G>A
NC_000011.10:g.6626164C>T
 06/18/2022 intron variant uncertain significance none provided

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

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002604331 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DCHS1 CLINVAR
OMIM 603057 CLINVAR