RGD:405111293 Rat Genome Database

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Variant: RGD:405111293 -  Homo sapiens

RGD ID: 405111293
ClinVar ID: CV3080828
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HFE  HFE-AS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 26,091,091
GRCh38 6 26,090,863
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_748t1:c.99C>T
NM_139010.3:c.77-1822C>T
NM_139011.3:c.77-2256C>T
NM_001406752.1:c.77-451C>T
More... 		10/27/2023 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003751602 CLINVAR
MedGen C0392514 CLINVAR
NCBI Gene HFE CLINVAR
  HFE-AS1 CLINVAR
OMIM 235200 CLINVAR
  613609 CLINVAR
SNOMED CT 35400008 CLINVAR