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rs121908082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908082(C;T)
Make rs121908082(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position1487841
GeneTPO
is asnp
is mentioned by
dbSNPrs121908082
ebirs121908082
HLIrs121908082
Exacrs121908082
Varsomers121908082
Maprs121908082
PheGenIrs121908082
hapmaprs121908082
1000 genomesrs121908082
hgdprs121908082
ensemblrs121908082
gopubmedrs121908082
geneviewrs121908082
scholarrs121908082
googlers121908082
pharmgkbrs121908082
gwascentralrs121908082
openSNPrs121908082
23andMers121908082
23andMe allrs121908082
SNP Nexus

SNPshotrs121908082
SNPdbers121908082
MSV3drs121908082
GWAS Ctlgrs121908082
Max Magnitude0
OMIM606765
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908082(G,T;G,T)
Alt rs121908082(G,T;G,T)
Reference rs121908082(C;C)
Significance Pathogenic
Disease Deficiency of iodide peroxidase
Variation info
Gene TPO
CLNDBN Deficiency of iodide peroxidase
Reversed 0
HGVS NC_000002.11:g.1491613C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004257.2,