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rs199752932

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199752932(A;G)
Make rs199752932(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position45097236
GeneDUOX2
is asnp
is mentioned by
dbSNPrs199752932
ebirs199752932
HLIrs199752932
Exacrs199752932
Varsomers199752932
Maprs199752932
PheGenIrs199752932
hapmaprs199752932
1000 genomesrs199752932
hgdprs199752932
ensemblrs199752932
gopubmedrs199752932
geneviewrs199752932
scholarrs199752932
googlers199752932
pharmgkbrs199752932
gwascentralrs199752932
openSNPrs199752932
23andMers199752932
23andMe allrs199752932
SNP Nexus

SNPshotrs199752932
SNPdbers199752932
MSV3drs199752932
GWAS Ctlgrs199752932
Max Magnitude0
ClinVar
Risk rs199752932(G;G)
Alt rs199752932(G;G)
Reference rs199752932(A;A)
Significance Probable-Pathogenic
Disease Thyroid dyshormonogenesis 6
Variation info
Gene DUOX2
CLNDBN Thyroid dyshormonogenesis 6
Reversed 0
HGVS NC_000015.9:g.45389434A>G
CLNSRC
CLNACC RCV000169658.1,