rs760903469 Rat Genome Database

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Variant: rs760903469 -  Homo sapiens

RGD ID: 152978756
RS ID: rs760903469
ClinVar ID: CV1673818
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADSS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 105,205,653
GRCh38 14 104,739,316
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_051175.1:g.20120G>A
NC_000014.9:g.104739316G>A
NC_000014.8:g.105205653G>A
NM_001320424.1:c.-240-12G>A
More... 		12/11/2023 intron variant benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:ADSS1
Accession:NM_001320424
Location:5UTRS;INTRON

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:XM_047430917
Location:INTRON

Gene Symbol:ADSS1
Accession:XM_047430916
Location:INTRON

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PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002236668 CLINVAR
dbSNP (RS) rs760903469 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ADSS1 CLINVAR
OMIM 612498 CLINVAR