rs1429670443 Rat Genome Database

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Variant: rs1429670443 -  Homo sapiens

RGD ID: 152091259
RS ID: rs1429670443
ClinVar ID: CV1629180
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SMAD2  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 18 45,377,638
GRCh38 18 47,851,267
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001135937.3:c.694+7T>A
NM_001003652.4:c.784+7T>A
NM_005901.6:c.784+7T>A
NG_029946.1:g.84878T>A
More... 		08/10/2023 intron variant likely benign|uncertain significance AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:SMAD2
Accession:NM_001135937
Location:INTRON

Gene Symbol:SMAD2
Accession:XM_047437508
Location:INTRON

Gene Symbol:SMAD2
Accession:NM_001003652
Location:INTRON

Gene Symbol:SMAD2
Accession:XM_047437507
Location:INTRON

Gene Symbol:SMAD2
Accession:XM_017025749
Location:INTRON

Gene Symbol:SMAD2
Accession:NM_005901
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002114106 CLINVAR
  RCV003331311 CLINVAR
dbSNP (RS) rs1429670443 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene SMAD2 CLINVAR
OMIM 601366 CLINVAR