rs371366387 Rat Genome Database

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Variant: rs371366387 -  Homo sapiens

RGD ID: 151815596
RS ID: rs371366387
ClinVar ID: CV1475789
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DUOX2  LOC127829453  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 45,394,190
GRCh38 15 45,101,992
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.2655-3C>T
NM_014080.5:c.2655-3C>T
NG_009447.1:g.17170C>T
NC_000015.10:g.45101992G>A
More... 		04/25/2022 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:DUOX2
Accession:NM_001363711
Location:INTRON

Gene Symbol:DUOX2
Accession:NM_014080
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001992253 CLINVAR
dbSNP (RS) rs371366387 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DUOX2 CLINVAR
OMIM 606759 CLINVAR