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rs121918688

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918688(C;C)
Make rs121918688(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24127623
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918688
ebirs121918688
HLIrs121918688
Exacrs121918688
Varsomers121918688
Maprs121918688
PheGenIrs121918688
hapmaprs121918688
1000 genomesrs121918688
hgdprs121918688
ensemblrs121918688
gopubmedrs121918688
geneviewrs121918688
scholarrs121918688
googlers121918688
pharmgkbrs121918688
gwascentralrs121918688
openSNPrs121918688
23andMers121918688
23andMe allrs121918688
SNP Nexus

SNPshotrs121918688
SNPdbers121918688
MSV3drs121918688
GWAS Ctlgrs121918688
Max Magnitude0
OMIM190160
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121918688(A,C;A,C)
Alt rs121918688(A,C;A,C)
Reference rs121918688(G;G)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized, autosomal dominant
Reversed 1
HGVS NC_000003.11:g.24169114C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013363.22,