rs368901021 Rat Genome Database

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Variant: rs368901021 -  Homo sapiens

RGD ID: 28891741
RS ID: rs368901021
ClinVar ID: CV873587
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DUOX2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 45,384,910
GRCh38 15 45,092,712
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.26450G>A
NC_000015.10:g.45092712C>T
NC_000015.9:g.45384910C>T
NM_014080.4:c.*1438G>A
More... 		01/13/2018 3 prime utr variant uncertain significance HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 6; THYROID HORMONOGENESIS, GENETIC DEFECT IN, 6
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DUOX2
Accession:NM_014080
Location:3UTRS;EXON

Gene Symbol:DUOX2
Accession:NM_001363711
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001121088 CLINVAR
dbSNP (RS) rs368901021 CLINVAR
MedGen C1846632 CLINVAR
NCBI Gene DUOX2 CLINVAR
OMIM 606759 CLINVAR
  607200 CLINVAR