RGD:150475935 Rat Genome Database

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Variant: RGD:150475935 -  Homo sapiens

RGD ID: 150475935
RS ID: rs2659873
ClinVar ID: CV1216738
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DCHS1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 6,650,856
GRCh38 11 6,629,625
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.5035+47A>G
NG_033858.2:g.31225A>G
NC_000011.10:g.6629625T>C
NC_000011.9:g.6650856T>C
 07/15/2018 intron variant benign none provided

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001616031 CLINVAR
dbSNP (RS) rs2659873 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DCHS1 CLINVAR
OMIM 603057 CLINVAR