RGD:11609118 Rat Genome Database

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Variant: RGD:11609118 -  Homo sapiens

RGD ID: 11609118
RS ID: rs2630336
ClinVar ID: CV322628
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004020  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 72,648,422
GRCh38 10 70,888,665
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008646.1:g.5120C>A
NC_000010.11:g.70888665G>T
NM_000281.2:c.-132C>A
NG_183466.1:g.334G>T
More... 		06/14/2016 2kb upstream variant benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000364283 CLINVAR
  RCV001541592 CLINVAR
dbSNP (RS) rs2630336 CLINVAR
MedGen C3661900 CLINVAR
  CN239229 CLINVAR
NCBI Gene LOC130004020 CLINVAR
  PCBD1 CLINVAR
OMIM 126090 CLINVAR