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rs121918709

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918709(A;G)
Make rs121918709(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24127634
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918709
ebirs121918709
HLIrs121918709
Exacrs121918709
Varsomers121918709
Maprs121918709
PheGenIrs121918709
hapmaprs121918709
1000 genomesrs121918709
hgdprs121918709
ensemblrs121918709
gopubmedrs121918709
geneviewrs121918709
scholarrs121918709
googlers121918709
pharmgkbrs121918709
gwascentralrs121918709
openSNPrs121918709
23andMers121918709
23andMe allrs121918709
SNP Nexus

SNPshotrs121918709
SNPdbers121918709
MSV3drs121918709
GWAS Ctlgrs121918709
Max Magnitude0
OMIM190160
Desc
Variant0040
Relatedalso
ClinVar
Risk rs121918709(G;G)
Alt rs121918709(G;G)
Reference rs121918709(A;A)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, selective pituitary
Reversed 1
HGVS NC_000003.11:g.24169125T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013397.23,