rs34803917 Rat Genome Database

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Variant: rs34803917 -  Homo sapiens

RGD ID: 150452336
RS ID: rs34803917
ClinVar ID: CV1220986
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 145,878,591
GRCh38 3 146,160,804
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.109+77C>T
NC_000003.12:g.146160804G>A
NC_000003.11:g.145878591G>A
NM_182943.3:c.109+77C>T
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 RCV001612080 CLINVAR
dbSNP (RS) rs34803917 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR