rs1555412892 Rat Genome Database

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Variant: rs1555412892 -  Homo sapiens

RGD ID: 13538674
RS ID: rs1555412892
ClinVar ID: CV504783
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DUOX2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 45,391,693
GRCh38 15 45,099,495
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009447.1:g.19667C>T
NC_000015.10:g.45099495G>A
NC_000015.9:g.45391693G>A
NM_014080.5:c.3416-13C>T
More... 		01/31/2017 intron variant likely benign AllHighlyPenetrant

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

Gene Symbol:DUOX2
Accession:NM_014080
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000612175 CLINVAR
dbSNP (RS) rs1555412892 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DUOX2 CLINVAR
OMIM 606759 CLINVAR