Rs121908883

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908883(A;A)
Make rs121908883(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143349
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908883
Exacrs121908883
PheGenIrs121908883
nextbiors121908883
hapmaprs121908883
1000 genomesrs121908883
hgdprs121908883
ensemblrs121908883
gopubmedrs121908883
geneviewrs121908883
scholarrs121908883
googlers121908883
pharmgkbrs121908883
gwascentralrs121908883
openSNPrs121908883
23andMers121908883
23andMe allrs121908883
SNP Nexus

SNPshotrs121908883
SNPdbers121908883
MSV3drs121908883
Max Magnitude0
OMIM603372
Desc
Variant0028
Relatedalso
ClinVar
Risk rs121908883(A;A)
Alt rs121908883(A;A)
Reference rs121908883(G;G)
Significance Pathogenic
Disease Hyperthyroidism
Variation info
Gene TSHR
CLNDBN Hyperthyroidism, nonautoimmune
Reversed 0
HGVS NC_000014.8:g.81609693G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006828.1,