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rs121918669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918669(G;T)
Make rs121918669(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position115033456
GeneTSHB
is asnp
is mentioned by
dbSNPrs121918669
ebirs121918669
HLIrs121918669
Exacrs121918669
Varsomers121918669
Maprs121918669
PheGenIrs121918669
hapmaprs121918669
1000 genomesrs121918669
hgdprs121918669
ensemblrs121918669
gopubmedrs121918669
geneviewrs121918669
scholarrs121918669
googlers121918669
pharmgkbrs121918669
gwascentralrs121918669
openSNPrs121918669
23andMers121918669
23andMe allrs121918669
SNP Nexus

SNPshotrs121918669
SNPdbers121918669
MSV3drs121918669
GWAS Ctlgrs121918669
Max Magnitude0
OMIM188540
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918669(A,T;A,T)
Alt rs121918669(A,T;A,T)
Reference rs121918669(G;G)
Significance Pathogenic
Disease Secondary hypothyroidism
Variation info
Gene TSHB
CLNDBN Secondary hypothyroidism
Reversed 0
HGVS NC_000001.10:g.115576077G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013522.22,