RGD:11599784 Rat Genome Database

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Variant: RGD:11599784 -  Homo sapiens

RGD ID: 11599784
RS ID: rs545046003
ClinVar ID: CV322616
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004020  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 72,648,386
GRCh38 10 70,888,629
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000010.11:g.70888629C>T
NM_000281.2:c.-96G>A
NG_008646.1:g.5156G>A
NC_000010.10:g.72648386C>T
More... 		06/14/2016 2kb upstream variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000268411 CLINVAR
dbSNP (RS) rs545046003 CLINVAR
MedGen CN239229 CLINVAR
NCBI Gene LOC130004020 CLINVAR
  PCBD1 CLINVAR
OMIM 126090 CLINVAR