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rs121918693

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918693(A;A)
Make rs121918693(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24127684
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918693
ebirs121918693
HLIrs121918693
Exacrs121918693
Varsomers121918693
Maprs121918693
PheGenIrs121918693
hapmaprs121918693
1000 genomesrs121918693
hgdprs121918693
ensemblrs121918693
gopubmedrs121918693
geneviewrs121918693
scholarrs121918693
googlers121918693
pharmgkbrs121918693
gwascentralrs121918693
openSNPrs121918693
23andMers121918693
23andMe allrs121918693
SNP Nexus

SNPshotrs121918693
SNPdbers121918693
MSV3drs121918693
GWAS Ctlgrs121918693
Max Magnitude0
OMIM190160
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121918693(A,T;A,T)
Alt rs121918693(A,T;A,T)
Reference rs121918693(G;G)
Significance Pathogenic
Disease Thyroid hormone resistance Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, selective pituitary Thyroid hormone resistance, generalized, autosomal dominant
Reversed 1
HGVS NC_000003.11:g.24169175C>A; NC_000003.11:g.24169175C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013390.16, RCV000013380.16,