Rs121908874

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908874(C;C)
Make rs121908874(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143584
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908874
Exacrs121908874
PheGenIrs121908874
nextbiors121908874
hapmaprs121908874
1000 genomesrs121908874
hgdprs121908874
ensemblrs121908874
gopubmedrs121908874
geneviewrs121908874
scholarrs121908874
googlers121908874
pharmgkbrs121908874
gwascentralrs121908874
openSNPrs121908874
23andMers121908874
23andMe allrs121908874
SNP Nexus

SNPshotrs121908874
SNPdbers121908874
MSV3drs121908874
Max Magnitude0
OMIM603372
Desc
Variant0019
Relatedalso
ClinVar
Risk rs121908874(C;C)
Alt rs121908874(C;C)
Reference rs121908874(T;T)
Significance Pathogenic
Disease Hyperthyroidism
Variation info
Gene TSHR
CLNDBN Hyperthyroidism, nonautoimmune
Reversed 0
HGVS NC_000014.8:g.81609928T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006818.1,