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rs121908088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908088(C;G)
Make rs121908088(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position1494011
GeneTPO
is asnp
is mentioned by
dbSNPrs121908088
ebirs121908088
HLIrs121908088
Exacrs121908088
Varsomers121908088
Maprs121908088
PheGenIrs121908088
hapmaprs121908088
1000 genomesrs121908088
hgdprs121908088
ensemblrs121908088
gopubmedrs121908088
geneviewrs121908088
scholarrs121908088
googlers121908088
pharmgkbrs121908088
gwascentralrs121908088
openSNPrs121908088
23andMers121908088
23andMe allrs121908088
SNP Nexus

SNPshotrs121908088
SNPdbers121908088
MSV3drs121908088
GWAS Ctlgrs121908088
GMAF0.0004591
Max Magnitude0
OMIM606765
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121908088(G;G)
Alt rs121908088(G;G)
Reference rs121908088(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.1497783C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004268.2,