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rs121908083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908083(G;G)
Make rs121908083(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position1484614
GeneLOC102723717, TPO
is asnp
is mentioned by
dbSNPrs121908083
ebirs121908083
HLIrs121908083
Exacrs121908083
Varsomers121908083
Maprs121908083
PheGenIrs121908083
hapmaprs121908083
1000 genomesrs121908083
hgdprs121908083
ensemblrs121908083
gopubmedrs121908083
geneviewrs121908083
scholarrs121908083
googlers121908083
pharmgkbrs121908083
gwascentralrs121908083
openSNPrs121908083
23andMers121908083
23andMe allrs121908083
SNP Nexus

SNPshotrs121908083
SNPdbers121908083
MSV3drs121908083
GWAS Ctlgrs121908083
Max Magnitude0
OMIM606765
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908083(G;G)
Alt rs121908083(G;G)
Reference rs121908083(T;T)
Significance Pathogenic
Disease Deficiency of iodide peroxidase
Variation info
Gene TPO
CLNDBN Deficiency of iodide peroxidase
Reversed 0
HGVS NC_000002.11:g.1488386T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004259.2,