RGD:408383634 Rat Genome Database

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Variant: RGD:408383634 -  Homo sapiens

RGD ID: 408383634
ClinVar ID: CV3525802
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 145,788,825
GRCh38 3 146,071,038
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.2058+4A>T
NM_182943.3:c.2121+4A>T
NG_009251.1:g.95458A>T
NC_000003.12:g.146071038T>A
More... 		08/31/2024 intron variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004766712 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR