rs746060894 Rat Genome Database

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Variant: rs746060894 -  Homo sapiens

RGD ID: 13540270
RS ID: rs746060894
ClinVar ID: CV507353
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: DYRK1A  
Reference Nucleotide: T
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 21 38,850,467
GRCh38 21 37,478,165
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001396.5:c.208-14del
NM_001347723.2:c.121-41del
NM_130438.2:c.208-14del
NM_001347722.2:c.208-41del
More... 		07/10/2017 intron variant likely benign AllHighlyPenetrant

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 RCV000614464 CLINVAR
dbSNP (RS) rs746060894 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DYRK1A CLINVAR
OMIM 600855 CLINVAR