RGD:12849041 Rat Genome Database

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Variant: RGD:12849041 -  Homo sapiens

RGD ID: 12849041
RS ID: rs185552165
ClinVar ID: CV363673
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GDI1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 153,666,858
GRCh38 X 154,438,512
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001493.3:c.46-11C>A
NG_008954.1:g.6600C>A
NC_000023.11:g.154438512C>A
NC_000023.10:g.153666858C>A
More... 		01/02/2017 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GDI1
Accession:NM_001493
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000423051 CLINVAR
dbSNP (RS) rs185552165 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GDI1 CLINVAR
OMIM 300104 CLINVAR