Rs121908864

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908864(C;C)
Make rs121908864(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143416
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908864
Exacrs121908864
PheGenIrs121908864
nextbiors121908864
hapmaprs121908864
1000 genomesrs121908864
hgdprs121908864
ensemblrs121908864
gopubmedrs121908864
geneviewrs121908864
scholarrs121908864
googlers121908864
pharmgkbrs121908864
gwascentralrs121908864
openSNPrs121908864
23andMers121908864
23andMe allrs121908864
SNP Nexus

SNPshotrs121908864
SNPdbers121908864
MSV3drs121908864
OMIM603372
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908864(C;C)
Alt rs121908864(C;C)
Reference rs121908864(T;T)
Significance Pathogenic
Disease Hyperthyroidism
Variation info
Gene TSHR
CLNDBN Hyperthyroidism, nonautoimmune
Reversed 0
HGVS NC_000014.8:g.81609760T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006806.1,