rs1700009371 Rat Genome Database

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Variant: rs1700009371 -  Homo sapiens

RGD ID: 151749860
RS ID: rs1700009371
ClinVar ID: CV1357275
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LARS2  LARS2-AS1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 45,537,766
GRCh38 3 45,496,274
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001368263.1:c.1524-1G>T
NM_015340.4:c.1524-1G>T
LRG_1353:g.112711G>T
NG_033907.3:g.112711G>T
More... 		11/01/2022 splice acceptor variant likely pathogenic|uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:LARS2
Accession:XM_047447829
Location:INTRON

Gene Symbol:LARS2
Accession:NM_001368263
Location:INTRON

Gene Symbol:LARS2
Accession:NM_015340
Location:INTRON

Gene Symbol:LARS2
Accession:XM_047447830
Location:INTRON

Gene Symbol:LARS2
Accession:XM_011533554
Location:INTRON

Gene Symbol:LARS2
Accession:XM_017006042
Location:INTRON

Gene Symbol:LARS2-AS1
Accession:NR_048543
Location:INTRON;NON-CODING

.
PMID:16199547   PMID:23541342   PMID:28492532   PMID:30737337  



Database
Acc Id
Source(s)
ClinVar RCV001872146 CLINVAR
dbSNP (RS) rs1700009371 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LARS2 CLINVAR
  LARS2-AS1 CLINVAR
OMIM 604544 CLINVAR