rs79024662 Rat Genome Database

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Variant: rs79024662 -  Homo sapiens

RGD ID: 150463827
RS ID: rs79024662
ClinVar ID: CV1273207
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 145,804,335
GRCh38 3 146,086,548
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.1127+239G>A
NM_182943.3:c.1127+239G>A
NG_009251.1:g.79948G>A
NC_000003.12:g.146086548C>T
More... 		10/01/2018 intron variant benign 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 RCV001693964 CLINVAR
dbSNP (RS) rs79024662 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR