rs143256118 Rat Genome Database

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Variant: rs143256118 -  Homo sapiens

RGD ID: 150486873
RS ID: rs143256118
ClinVar ID: CV1203368
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: SMAD2  
Reference Nucleotide: A
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 18 45,394,845
GRCh38 18 47,868,474
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001135937.3:c.431-16del
NM_001003652.4:c.521-16del
NM_005901.6:c.521-16del
NG_029946.1:g.67672del
More... 		01/31/2024 intron variant benign|likely benign AllHighlyPenetrant; none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV001591546 CLINVAR
  RCV003323908 CLINVAR
dbSNP (RS) rs143256118 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene SMAD2 CLINVAR
OMIM 601366 CLINVAR