rs2427613 Rat Genome Database

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Variant: rs2427613 -  Homo sapiens

RGD ID: 15121156
RS ID: rs2427613
ClinVar ID: CV780153
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYT1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 62,830,279
GRCh38 20 64,198,926
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_004535.3:c.55+10G>A
NC_000020.11:g.64198926G>A
NC_000020.10:g.62830279G>A
NM_004535.2:c.55+10G>A
 12/31/2019 intron variant benign MYT1-related condition; none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:MYT1
Accession:NM_004535
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV000962840 CLINVAR
  RCV003926188 CLINVAR
dbSNP (RS) rs2427613 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYT1 CLINVAR
OMIM 600379 CLINVAR