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rs199589510

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199589510(A;A)
Make rs199589510(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position45103961
GeneDUOX2
is asnp
is mentioned by
dbSNPrs199589510
dbSNP (old)rs199589510
ClinGenrs199589510
ebirs199589510
HLIrs199589510
Exacrs199589510
Gnomadrs199589510
Varsomers199589510
LitVarrs199589510
Maprs199589510
PheGenIrs199589510
Biobankrs199589510
1000 genomesrs199589510
hgdprs199589510
ensemblrs199589510
gopubmedrs199589510
geneviewrs199589510
scholarrs199589510
googlers199589510
pharmgkbrs199589510
gwascentralrs199589510
openSNPrs199589510
23andMers199589510
23andMe allrs199589510
SNPshotrs199589510
SNPdbers199589510
MSV3drs199589510
GWAS Ctlgrs199589510
Max Magnitude0
ClinVar
Risk rs199589510(A;A)
Alt rs199589510(A;A)
Reference Rs199589510(G;G)
Significance Probable-Pathogenic
Disease Thyroid dyshormonogenesis 6
Variation info
Gene DUOX2
CLNDBN Thyroid dyshormonogenesis 6
Reversed 0
HGVS NC_000015.9:g.45396159G>A
CLNSRC
CLNACC RCV000490414.1,