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rs121918670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918670(C;T)
Make rs121918670(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position115034015
GeneTSHB
is asnp
is mentioned by
dbSNPrs121918670
ebirs121918670
HLIrs121918670
Exacrs121918670
Varsomers121918670
Maprs121918670
PheGenIrs121918670
hapmaprs121918670
1000 genomesrs121918670
hgdprs121918670
ensemblrs121918670
gopubmedrs121918670
geneviewrs121918670
scholarrs121918670
googlers121918670
pharmgkbrs121918670
gwascentralrs121918670
openSNPrs121918670
23andMers121918670
23andMe allrs121918670
SNP Nexus

SNPshotrs121918670
SNPdbers121918670
MSV3drs121918670
GWAS Ctlgrs121918670
Max Magnitude0
OMIM188540
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121918670(T;T)
Alt rs121918670(T;T)
Reference rs121918670(C;C)
Significance Pathogenic
Disease Secondary hypothyroidism
Variation info
Gene TSHB
CLNDBN Secondary hypothyroidism
Reversed 0
HGVS NC_000001.10:g.115576636C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013524.22,