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rs119472028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119472028(C;T)
Make rs119472028(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position45104176
GeneDUOX2
is asnp
is mentioned by
dbSNPrs119472028
ebirs119472028
HLIrs119472028
Exacrs119472028
Varsomers119472028
Maprs119472028
PheGenIrs119472028
hapmaprs119472028
1000 genomesrs119472028
hgdprs119472028
ensemblrs119472028
gopubmedrs119472028
geneviewrs119472028
scholarrs119472028
googlers119472028
pharmgkbrs119472028
gwascentralrs119472028
openSNPrs119472028
23andMers119472028
23andMe allrs119472028
SNP Nexus

SNPshotrs119472028
SNPdbers119472028
MSV3drs119472028
GWAS Ctlgrs119472028
Max Magnitude0
OMIM606759
Desc
Variant0003
Relatedalso
ClinVar
Risk rs119472028(T;T)
Alt rs119472028(T;T)
Reference rs119472028(C;C)
Significance Pathogenic
Disease Thyroid dyshormonogenesis 6
Variation info
Gene DUOX2
CLNDBN Thyroid dyshormonogenesis 6
Reversed 1
HGVS NC_000015.9:g.45396374G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004279.2,