RGD:11579982 Rat Genome Database

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Variant: RGD:11579982 -  Homo sapiens

RGD ID: 11579982
RS ID: rs555618086
ClinVar ID: CV281389
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DHCR24  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 55,330,965
GRCh38 1 54,865,292
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_008839.1:g.26957G>A
NC_000001.11:g.54865292C>T
NC_000001.10:g.55330965C>T
NM_014762.4:c.1020+11G>A
More... 		01/13/2018 intron variant likely benign|uncertain significance antenatal <1 / 1 000 000
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DHCR24
Accession:NM_014762
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000319041 CLINVAR
dbSNP (RS) rs555618086 CLINVAR
MedGen C1865596 CLINVAR
NCBI Gene DHCR24 CLINVAR
OMIM 602398 CLINVAR
  606418 CLINVAR