RGD:156015409 Rat Genome Database

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Variant: RGD:156015409 -  Homo sapiens

RGD ID: 156015409
ClinVar ID: CV2121355
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LARS2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 45,488,477
GRCh38 3 45,446,985
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1353t1:c.606+5G>A
NM_001368263.1:c.606+5G>A
NM_015340.4:c.606+5G>A
LRG_1353:g.63422G>A
More... 		08/20/2024 intron variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:LARS2
Accession:NM_001368263
Location:INTRON

Gene Symbol:LARS2
Accession:XM_017006042
Location:INTRON

Gene Symbol:LARS2
Accession:XM_047447829
Location:INTRON

Gene Symbol:LARS2
Accession:XM_011533554
Location:INTRON

Gene Symbol:LARS2
Accession:XM_047447830
Location:INTRON

Gene Symbol:LARS2
Accession:NM_015340
Location:INTRON

.
PMID:9536098   PMID:17576681   PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002948505 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LARS2 CLINVAR
OMIM 604544 CLINVAR