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rs121918668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918668(A;A)
Make rs121918668(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position115033507
GeneTSHB
is asnp
is mentioned by
dbSNPrs121918668
ebirs121918668
HLIrs121918668
Exacrs121918668
Varsomers121918668
Maprs121918668
PheGenIrs121918668
hapmaprs121918668
1000 genomesrs121918668
hgdprs121918668
ensemblrs121918668
gopubmedrs121918668
geneviewrs121918668
scholarrs121918668
googlers121918668
pharmgkbrs121918668
gwascentralrs121918668
openSNPrs121918668
23andMers121918668
23andMe allrs121918668
SNP Nexus

SNPshotrs121918668
SNPdbers121918668
MSV3drs121918668
GWAS Ctlgrs121918668
Max Magnitude0
OMIM188540
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918668(A;A)
Alt rs121918668(A;A)
Reference rs121918668(G;G)
Significance Pathogenic
Disease Secondary hypothyroidism
Variation info
Gene TSHB
CLNDBN Secondary hypothyroidism
Reversed 0
HGVS NC_000001.10:g.115576128G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013521.24,