RGD:13836355 Rat Genome Database

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Variant: RGD:13836355 -  Homo sapiens

RGD ID: 13836355
RS ID: rs373514835
ClinVar ID: CV587628
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP7A1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 59,409,157
GRCh38 8 58,496,598
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000780.4:c.908+6T>G
NG_007969.1:g.8565T>G
NC_000008.11:g.58496598A>C
NC_000008.10:g.59409157A>C
 03/19/2018 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:CYP7A1
Accession:NM_000780
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000732445 CLINVAR
dbSNP (RS) rs373514835 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene CYP7A1 CLINVAR
OMIM 118455 CLINVAR