rs8134408 Rat Genome Database

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Variant: rs8134408 -  Homo sapiens

RGD ID: 14710955
RS ID: rs8134408
ClinVar ID: CV670629
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DYRK1A  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 21 38,868,111
GRCh38 21 37,495,809
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001347721.2:c.1072-309A>T
NM_130436.2:c.1072-309A>T
NM_001347723.2:c.985-309A>T
NM_001396.5:c.1099-309A>T
More... 		06/19/2018 intron variant benign none provided

Gene Symbol:DYRK1A
Accession:NM_101395
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_130436
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_130438
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_001396
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_001347722
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_001347721
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_001347723
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV000827875 CLINVAR
dbSNP (RS) rs8134408 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DYRK1A CLINVAR
OMIM 600855 CLINVAR