RGD:405114681 Rat Genome Database

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Variant: RGD:405114681 -  Homo sapiens

RGD ID: 405114681
ClinVar ID: CV2992166
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HFE  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 26,091,786
GRCh38 6 26,091,558
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008720.2:g.9278G>A
NC_000006.12:g.26091558G>A
NC_000006.11:g.26091786G>A
NM_000410.3:c.585G>A
More... 		02/10/2023 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 RCV003752086 CLINVAR
MedGen C0392514 CLINVAR
NCBI Gene HFE CLINVAR
OMIM 235200 CLINVAR
  613609 CLINVAR
SNOMED CT 35400008 CLINVAR