RGD:401908555 Rat Genome Database

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Variant: RGD:401908555 -  Homo sapiens

RGD ID: 401908555
ClinVar ID: CV2811664
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 13,710,658
GRCh38 19 13,599,844
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000019.9:g.13710658G>A
NC_000019.10:g.13599844G>A
10/01/2023 likely benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003423370 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CACNA1A CLINVAR
OMIM 601011 CLINVAR