rs374567883 Rat Genome Database

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Variant: rs374567883 -  Homo sapiens

RGD ID: 150551329
RS ID: rs374567883
ClinVar ID: CV1297305
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 145,790,452
GRCh38 3 146,072,665
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.1681C>G
NM_182943.3:c.1744C>G
NG_009251.1:g.93831C>G
NC_000003.12:g.146072665G>C
More... 		05/20/2019 missense variant uncertain significance none provided

Gene Symbol:PLOD2
Accession:NM_000935
Location:INTRON

Gene Symbol:PLOD2
Accession:NM_182943
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_017006625
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_047448319
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_047448320
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001766987 CLINVAR
dbSNP (RS) rs374567883 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR