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rs121908084

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908084(A;A)
Make rs121908084(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position1487991
GeneTPO
is asnp
is mentioned by
dbSNPrs121908084
ebirs121908084
HLIrs121908084
Exacrs121908084
Varsomers121908084
Maprs121908084
PheGenIrs121908084
hapmaprs121908084
1000 genomesrs121908084
hgdprs121908084
ensemblrs121908084
gopubmedrs121908084
geneviewrs121908084
scholarrs121908084
googlers121908084
pharmgkbrs121908084
gwascentralrs121908084
openSNPrs121908084
23andMers121908084
23andMe allrs121908084
SNP Nexus

SNPshotrs121908084
SNPdbers121908084
MSV3drs121908084
GWAS Ctlgrs121908084
Max Magnitude0
OMIM606765
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908084(A;A)
Alt rs121908084(A;A)
Reference Rs121908084(G;G)
Significance Pathogenic
Disease Deficiency of iodide peroxidase
Variation info
Gene TPO
CLNDBN Deficiency of iodide peroxidase
Reversed 0
HGVS NC_000002.11:g.1491763G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004260.3,