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rs180671269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180671269(A;A)
Make rs180671269(A;T)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position45107450
GeneDUOX2
is asnp
is mentioned by
dbSNPrs180671269
dbSNP (old)rs180671269
ClinGenrs180671269
ebirs180671269
HLIrs180671269
Exacrs180671269
Gnomadrs180671269
Varsomers180671269
Maprs180671269
PheGenIrs180671269
Biobankrs180671269
1000 genomesrs180671269
hgdprs180671269
ensemblrs180671269
gopubmedrs180671269
geneviewrs180671269
scholarrs180671269
googlers180671269
pharmgkbrs180671269
gwascentralrs180671269
openSNPrs180671269
23andMers180671269
23andMe allrs180671269
SNPshotrs180671269
SNPdbers180671269
MSV3drs180671269
GWAS Ctlgrs180671269
Max Magnitude0
ClinVar
Risk rs180671269(A;A) rs180671269(C;C)
Alt rs180671269(A;A) rs180671269(C;C)
Reference Rs180671269(T;T)
Significance Pathogenic
Disease Thyroid dyshormonogenesis 6
Variation info
Gene DUOX2
CLNDBN Thyroid dyshormonogenesis 6
Reversed 0
HGVS NC_000015.9:g.45399648T>A
CLNSRC
CLNACC RCV000329453.1,