rs755626653 Rat Genome Database

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Variant: rs755626653 -  Homo sapiens

RGD ID: 152036298
RS ID: rs755626653
ClinVar ID: CV1617519
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: SMAD2  
Reference Nucleotide: -
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 18 45,375,076
GRCh38 18 47,848,705
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005901.6:c.785-18dup
NM_001135937.3:c.695-18dup
NM_001003652.4:c.785-18dup
NG_029946.1:g.87440dup
More... 		01/28/2024 intron variant benign AllHighlyPenetrant; none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002125383 CLINVAR
  RCV003323992 CLINVAR
dbSNP (RS) rs755626653 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene SMAD2 CLINVAR
OMIM 601366 CLINVAR