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rs121918694

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918694(A;A)
Make rs121918694(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24143539
GeneLOC101927854, THRB
is asnp
is mentioned by
dbSNPrs121918694
ebirs121918694
HLIrs121918694
Exacrs121918694
Varsomers121918694
Maprs121918694
PheGenIrs121918694
hapmaprs121918694
1000 genomesrs121918694
hgdprs121918694
ensemblrs121918694
gopubmedrs121918694
geneviewrs121918694
scholarrs121918694
googlers121918694
pharmgkbrs121918694
gwascentralrs121918694
openSNPrs121918694
23andMers121918694
23andMe allrs121918694
SNP Nexus

SNPshotrs121918694
SNPdbers121918694
MSV3drs121918694
GWAS Ctlgrs121918694
Max Magnitude0
OMIM190160
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121918694(A;A)
Alt rs121918694(A;A)
Reference rs121918694(G;G)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene LOC101927854 THRB
CLNDBN Thyroid hormone resistance, generalized, autosomal dominant
Reversed 1
HGVS NC_000003.11:g.24185030C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013381.16,