rs779694346 Rat Genome Database

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Variant: rs779694346 -  Homo sapiens

RGD ID: 152114807
RS ID: rs779694346
ClinVar ID: CV1628115
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLOD2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 145,802,939
GRCh38 3 146,085,152
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_000935.3:c.1232+17G>A
NM_182943.3:c.1232+17G>A
NG_009251.1:g.81344G>A
NC_000003.12:g.146085152C>T
More... 		10/13/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

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:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002197254 CLINVAR
dbSNP (RS) rs779694346 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLOD2 CLINVAR
OMIM 601865 CLINVAR