Rs121908876

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908876(A;A)
Make rs121908876(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143572
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908876
PheGenIrs121908876
nextbiors121908876
hapmaprs121908876
1000 genomesrs121908876
hgdprs121908876
ensemblrs121908876
gopubmedrs121908876
geneviewrs121908876
scholarrs121908876
googlers121908876
pharmgkbrs121908876
gwascentralrs121908876
openSNPrs121908876
23andMers121908876
23andMe allrs121908876
SNP Nexus

SNPshotrs121908876
SNPdbers121908876
MSV3drs121908876
Max Magnitude0
OMIM603372
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121908876(A;A)
Alt rs121908876(A;A)
Reference rs121908876(G;G)
Significance Pathogenic
Disease Hyperthyroidism
Variation info
Gene TSHR
CLNDBN Hyperthyroidism, nonautoimmune
Reversed 0
HGVS NC_000014.8:g.81609916G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006820.1,