RGD:150480619 Rat Genome Database

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Variant: RGD:150480619 -  Homo sapiens

RGD ID: 150480619
RS ID: rs73959247
ClinVar ID: CV1239617
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 135,809,572
GRCh38 2 135,052,002
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_016972.1:g.4738T>G
NC_000002.12:g.135052002T>G
NC_000002.11:g.135809572T>G
 06/26/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001652780 CLINVAR
dbSNP (RS) rs73959247 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RAB3GAP1 CLINVAR
OMIM 602536 CLINVAR