rs370012799 Rat Genome Database

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Variant: rs370012799 -  Homo sapiens

RGD ID: 152985123
RS ID: rs370012799
ClinVar ID: CV1673904
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADSS1  LOC127828852  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 105,209,539
GRCh38 14 104,743,202
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_152328.5:c.1073+11C>A
NM_199165.2:c.1202+11C>A
NM_001320424.1:c.458+11C>A
NG_051175.1:g.24006C>A
More... 		12/12/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:ADSS1
Accession:NM_152328
Location:INTRON

Gene Symbol:ADSS1
Accession:NM_199165
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_006720026
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_011536412
Location:INTRON

Gene Symbol:ADSS1
Accession:NM_001320424
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_047430917
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_047430916
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002239761 CLINVAR
dbSNP (RS) rs370012799 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ADSS1 CLINVAR
OMIM 612498 CLINVAR