rs587688778 Rat Genome Database

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Variant: rs587688778 -  Homo sapiens

RGD ID: 11625311
RS ID: rs587688778
ClinVar ID: CV325097
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130006761  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 111,896,040
GRCh38 11 112,025,316
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Age of Onset
Trait Synonyms
NG_013342.1:g.5503G>A
NC_000011.10:g.112025316G>A
NC_000011.9:g.111896040G>A
 10/09/2018 5 prime utr variant likely benign neonatal/infancy none provided

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001581459 CLINVAR
dbSNP (RS) rs587688778 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DLAT CLINVAR
  LOC130006761 CLINVAR
OMIM 608770 CLINVAR