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rs119472027

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119472027(C;T)
Make rs119472027(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position45106217
GeneDUOX2
is asnp
is mentioned by
dbSNPrs119472027
ebirs119472027
HLIrs119472027
Exacrs119472027
Varsomers119472027
Maprs119472027
PheGenIrs119472027
hapmaprs119472027
1000 genomesrs119472027
hgdprs119472027
ensemblrs119472027
gopubmedrs119472027
geneviewrs119472027
scholarrs119472027
googlers119472027
pharmgkbrs119472027
gwascentralrs119472027
openSNPrs119472027
23andMers119472027
23andMe allrs119472027
SNP Nexus

SNPshotrs119472027
SNPdbers119472027
MSV3drs119472027
GWAS Ctlgrs119472027
Max Magnitude0
OMIM606759
Desc
Variant0002
Relatedalso
ClinVar
Risk rs119472027(T;T)
Alt rs119472027(T;T)
Reference rs119472027(C;C)
Significance Pathogenic
Disease Thyroid dyshormonogenesis 6
Variation info
Gene DUOX2
CLNDBN Thyroid dyshormonogenesis 6
Reversed 1
HGVS NC_000015.9:g.45398415G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004278.2,