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rs119472026

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119472026(C;T)
Make rs119472026(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position45108887
GeneDUOX2
is asnp
is mentioned by
dbSNPrs119472026
ebirs119472026
HLIrs119472026
Exacrs119472026
Varsomers119472026
Maprs119472026
PheGenIrs119472026
hapmaprs119472026
1000 genomesrs119472026
hgdprs119472026
ensemblrs119472026
gopubmedrs119472026
geneviewrs119472026
scholarrs119472026
googlers119472026
pharmgkbrs119472026
gwascentralrs119472026
openSNPrs119472026
23andMers119472026
23andMe allrs119472026
SNP Nexus

SNPshotrs119472026
SNPdbers119472026
MSV3drs119472026
GWAS Ctlgrs119472026
Max Magnitude0
OMIM606759
Desc
Variant0001
Relatedalso
ClinVar
Risk rs119472026(T;T)
Alt rs119472026(T;T)
Reference rs119472026(C;C)
Significance Pathogenic
Disease Thyroid dyshormonogenesis 6
Variation info
Gene DUOX2
CLNDBN Thyroid dyshormonogenesis 6
Reversed 1
HGVS NC_000015.9:g.45401085G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004277.2,