RGD:402475673 Rat Genome Database

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Variant: RGD:402475673 -  Homo sapiens

RGD ID: 402475673
ClinVar ID: CV2857034
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 145,820,533
GRCh38 3 146,102,746
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.777+9C>T
NM_182943.3:c.777+9C>T
NG_009251.1:g.63750C>T
NC_000003.12:g.146102746G>A
More... 		11/13/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:PLOD2
Accession:XM_017006625
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_047448319
Location:INTRON

Gene Symbol:PLOD2
Accession:NM_000935
Location:INTRON

Gene Symbol:PLOD2
Accession:NM_182943
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_047448320
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003543330 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR