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rs121917847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917847(C;T)
Make rs121917847(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position109087561
GeneTRHR
is asnp
is mentioned by
dbSNPrs121917847
ebirs121917847
HLIrs121917847
Exacrs121917847
Varsomers121917847
Maprs121917847
PheGenIrs121917847
hapmaprs121917847
1000 genomesrs121917847
hgdprs121917847
ensemblrs121917847
gopubmedrs121917847
geneviewrs121917847
scholarrs121917847
googlers121917847
pharmgkbrs121917847
gwascentralrs121917847
openSNPrs121917847
23andMers121917847
23andMe allrs121917847
SNP Nexus

SNPshotrs121917847
SNPdbers121917847
MSV3drs121917847
GWAS Ctlgrs121917847
Max Magnitude0
ClinVar
Risk rs121917847(T;T)
Alt rs121917847(T;T)
Reference rs121917847(C;C)
Significance Pathogenic
Disease Thyrotropin-releasing hormone resistance
Variation info
Gene TRHR
CLNDBN Thyrotropin-releasing hormone resistance, generalized
Reversed 0
HGVS NC_000008.10:g.110099790C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013519.24,