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rs119472029

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119472029(C;T)
Make rs119472029(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position45109895
GeneDUOX2
is asnp
is mentioned by
dbSNPrs119472029
ebirs119472029
HLIrs119472029
Exacrs119472029
Varsomers119472029
Maprs119472029
PheGenIrs119472029
hapmaprs119472029
1000 genomesrs119472029
hgdprs119472029
ensemblrs119472029
gopubmedrs119472029
geneviewrs119472029
scholarrs119472029
googlers119472029
pharmgkbrs119472029
gwascentralrs119472029
openSNPrs119472029
23andMers119472029
23andMe allrs119472029
SNP Nexus

SNPshotrs119472029
SNPdbers119472029
MSV3drs119472029
GWAS Ctlgrs119472029
Max Magnitude0
OMIM606759
Desc
Variant0004
Relatedalso
ClinVar
Risk rs119472029(T;T)
Alt rs119472029(T;T)
Reference rs119472029(C;C)
Significance Pathogenic
Disease Thyroid dyshormonogenesis 6
Variation info
Gene DUOX2
CLNDBN Thyroid dyshormonogenesis 6
Reversed 1
HGVS NC_000015.9:g.45402093G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004280.3,