rs7639592 Rat Genome Database

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Variant: rs7639592 -  Homo sapiens

RGD ID: 150505107
RS ID: rs7639592
ClinVar ID: CV1286104
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 145,790,948
GRCh38 3 146,073,161
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.1680+126T>C
NM_182943.3:c.1743+126T>C
NG_009251.1:g.93335T>C
NC_000003.12:g.146073161A>G
More... 		06/26/2018 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

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001719527 CLINVAR
dbSNP (RS) rs7639592 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR