RGD:11664065 Rat Genome Database

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Variant: RGD:11664065 -  Homo sapiens

RGD ID: 11664065
RS ID: rs886062591
ClinVar ID: CV307498
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126860302  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 11,351,835
GRCh38 8 11,494,326
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.11494326C>T
NC_000008.10:g.11351835C>T
NG_023543.2:g.5315C>T
NG_084802.2:g.1347C>T
More... 		06/14/2016 5 prime utr variant uncertain significance Mason type diabetes
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000402101 CLINVAR
dbSNP (RS) rs886062591 CLINVAR
MedGen C0342276 CLINVAR
NCBI Gene BLK CLINVAR
  LOC126860302 CLINVAR
OMIM 191305 CLINVAR
  606391 CLINVAR
SNOMED CT 28453007 CLINVAR