rs2144276111 Rat Genome Database

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Variant: rs2144276111 -  Homo sapiens

RGD ID: 151845146
RS ID: rs2144276111
ClinVar ID: CV1359694
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: SMAD2  
Reference Nucleotide: A
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 18 45,368,216
GRCh38 18 47,841,845
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001135937.3:c.1297del
NM_001003652.4:c.1387del
NM_005901.6:c.1387del
NG_029946.1:g.94301del
More... 		04/14/2021 frameshift variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002032301 CLINVAR
dbSNP (RS) rs2144276111 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SMAD2 CLINVAR
OMIM 601366 CLINVAR