Rs121908878

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Merged intors121908873
Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908878(A;A)
Make rs121908878(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position81139828
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908878
PheGenIrs121908878
nextbiors121908878
hapmaprs121908878
1000 genomesrs121908878
hgdprs121908878
ensemblrs121908878
gopubmedrs121908878
geneviewrs121908878
scholarrs121908878
googlers121908878
pharmgkbrs121908878
gwascentralrs121908878
openSNPrs121908878
23andMers121908878
23andMe allrs121908878
SNP Nexus

SNPshotrs121908878
SNPdbers121908878
MSV3drs121908878
StatusMerged into rs121908873
Max Magnitude0
OMIM603372
Desc
Variant0023
Relatedalso
ClinVar
Risk rs121908878(A;A)
Alt rs121908878(A;A)
Reference rs121908878(G;G)
Significance Pathogenic
Disease Hyperthyroidism
Variation info
Gene TSHR
CLNDBN Hyperthyroidism, nonautoimmune
Reversed 0
HGVS NC_000014.8:g.81606172G>A
CLNSRC OMIM Allelic Variant
CLNACC SCV000027019.1,