RGD:408378334 Rat Genome Database

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Variant: RGD:408378334 -  Homo sapiens

RGD ID: 408378334
ClinVar ID: CV3512074
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 145,803,054
GRCh38 3 146,085,267
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.1134T>C
NM_182943.3:c.1134T>C
NG_009251.1:g.81229T>C
NC_000003.12:g.146085267A>G
More... 		03/05/2019 synonymous variant likely benign PLOD2-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004752218 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR