rs73406335 Rat Genome Database

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Variant: rs73406335 -  Homo sapiens

RGD ID: 150452829
RS ID: rs73406335
ClinVar ID: CV1219763
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DUOX2  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 45,398,231
GRCh38 15 45,106,033
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001363711.2:c.2148+92A>C
NM_014080.5:c.2148+92A>C
NG_009447.1:g.13129A>C
NC_000015.10:g.45106033T>G
More... 		07/09/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DUOX2
Accession:NM_014080
Location:INTRON

Gene Symbol:DUOX2
Accession:NM_001363711
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001612144 CLINVAR
dbSNP (RS) rs73406335 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DUOX2 CLINVAR
OMIM 606759 CLINVAR