RGD:405119492 Rat Genome Database

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Variant: RGD:405119492 -  Homo sapiens

RGD ID: 405119492
ClinVar ID: CV3131377
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: G6PD  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 153,761,299
GRCh38 X 154,533,084
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001042351.3:c.909G>A
NM_001360016.2:c.909G>A
NM_000402.4:c.999G>A
NG_009015.2:g.19489G>A
More... 		10/25/2023 synonymous variant likely benign Class I glucose-6-phosphate dehydrogenase deficiency; Favism, susceptibility to; Hemolytic anemia due to G6PD deficiency
Disease Annotations     Click to see Annotation Detail View
favism  (IAGP)


Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003837241 CLINVAR
MedGen C2720289 CLINVAR
NCBI Gene G6PD CLINVAR
OMIM 300908 CLINVAR
  305900 CLINVAR