RGD:401906995 Rat Genome Database

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Variant: RGD:401906995 -  Homo sapiens

RGD ID: 401906995
ClinVar ID: CV2811663
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 13,710,656
GRCh38 19 13,599,842
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000019.10:g.13599842C>A
NC_000019.9:g.13710656C>A
06/01/2022 likely benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003421863 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CACNA1A CLINVAR
OMIM 601011 CLINVAR