RGD:11665335 Rat Genome Database

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Variant: RGD:11665335 -  Homo sapiens

RGD ID: 11665335
RS ID: rs10900296
ClinVar ID: CV353127
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC106736614  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 43,572,507
GRCh38 10 43,077,059
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
LRG_518:g.4991A>G
NG_007489.1:g.4991A>G
NC_000010.11:g.43077059A>G
NC_000010.10:g.43572507A>G
More... 		06/24/2018 2kb upstream variant|5 prime utr variant benign antenatal|childhood 1-5 / 10 000|1-9 / 1 000 000 Chromaffin cell tumor; Chromaffin paraganglioma; Chromaffin tumor; Chromaffinoma; HEREDITARY RENAL APLASIA; Medullary paraganglioma; none provided; RENAL APLASIA; Urogenital adysplasia, hereditary
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000265906 CLINVAR
  RCV000281211 CLINVAR
  RCV000320981 CLINVAR
  RCV000375701 CLINVAR
  RCV001692084 CLINVAR
dbSNP (RS) rs10900296 CLINVAR
MedGen C0027662 CLINVAR
  C0031511 CLINVAR
  C1619700 CLINVAR
  C3661900 CLINVAR
  CN239304 CLINVAR
NCBI Gene 106736614 CLINVAR
  RET CLINVAR
OMIM 164761 CLINVAR
  171300 CLINVAR
  191830 CLINVAR
SNOMED CT 46724008 CLINVAR