Rs121908879

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908879(A;G)
Make rs121908879(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position81096641
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs121908879
Exacrs121908879
PheGenIrs121908879
nextbiors121908879
hapmaprs121908879
1000 genomesrs121908879
hgdprs121908879
ensemblrs121908879
gopubmedrs121908879
geneviewrs121908879
scholarrs121908879
googlers121908879
pharmgkbrs121908879
gwascentralrs121908879
openSNPrs121908879
23andMers121908879
23andMe allrs121908879
SNP Nexus

SNPshotrs121908879
SNPdbers121908879
MSV3drs121908879
Max Magnitude0
OMIM603372
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121908879(G;G)
Alt rs121908879(G;G)
Reference rs121908879(A;A)
Significance Pathogenic
Disease Hyperthyroidism
Variation info
Gene TSHR
CLNDBN Hyperthyroidism, familial gestational
Reversed 0
HGVS NC_000014.8:g.81562985A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006824.1,