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rs121918700

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918700(C;C)
Make rs121918700(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24127679
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918700
ebirs121918700
HLIrs121918700
Exacrs121918700
Varsomers121918700
Maprs121918700
PheGenIrs121918700
hapmaprs121918700
1000 genomesrs121918700
hgdprs121918700
ensemblrs121918700
gopubmedrs121918700
geneviewrs121918700
scholarrs121918700
googlers121918700
pharmgkbrs121918700
gwascentralrs121918700
openSNPrs121918700
23andMers121918700
23andMe allrs121918700
SNP Nexus

SNPshotrs121918700
SNPdbers121918700
MSV3drs121918700
GWAS Ctlgrs121918700
Max Magnitude0
OMIM190160
Desc
Variant0027
Relatedalso
ClinVar
Risk rs121918700(C;C)
Alt rs121918700(C;C)
Reference rs121918700(G;G)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized
Reversed 1
HGVS NC_000003.11:g.24169170C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013368.24,