rs199536527 Rat Genome Database

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Variant: rs199536527 -  Homo sapiens

RGD ID: 127323011
RS ID: rs199536527
ClinVar ID: CV1157466
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DUOX2  LOC127829455  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 45,404,737
GRCh38 15 45,112,539
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.325+15G>A
NM_014080.5:c.325+15G>A
NG_016992.1:g.3215C>T
NG_009447.1:g.6623G>A
More... 		01/28/2024 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:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001523768 CLINVAR
dbSNP (RS) rs199536527 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DUOX2 CLINVAR
OMIM 606759 CLINVAR