rs202042741 Rat Genome Database

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Variant: rs202042741 -  Homo sapiens

RGD ID: 150443709
RS ID: rs202042741
ClinVar ID: CV1205166
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: PLOD2  
Reference Nucleotide: T
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 3 145,790,187
GRCh38 3 146,072,400
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.1785+162del
NM_182943.3:c.1848+162del
NG_009251.1:g.94097del
NC_000003.12:g.146072400del
More... 		07/21/2018 intron variant likely benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV001584009 CLINVAR
dbSNP (RS) rs202042741 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR