rs6802384 Rat Genome Database

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Variant: rs6802384 -  Homo sapiens

RGD ID: 14727295
RS ID: rs6802384
ClinVar ID: CV659733
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 145,841,854
GRCh38 3 146,124,067
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.201+71A>G
NM_182943.3:c.201+71A>G
NG_009251.1:g.42429A>G
NC_000003.12:g.146124067T>C
More... 		06/14/2018 intron variant benign none provided

Gene Symbol:PLOD2
Accession:XM_017006625
Location:5UTRS;INTRON

Gene Symbol:PLOD2
Accession:XM_047448319
Location:5UTRS;INTRON

Gene Symbol:PLOD2
Accession:NM_000935
Location:INTRON

Gene Symbol:PLOD2
Accession:NM_182943
Location:INTRON

Gene Symbol:PLOD2
Accession:XM_047448320
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV000834250 CLINVAR
dbSNP (RS) rs6802384 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR