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rs121908873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121908873(G;T)
Make rs121908873(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81139828
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908873
ebirs121908873
HLIrs121908873
Exacrs121908873
Varsomers121908873
Maprs121908873
PheGenIrs121908873
hapmaprs121908873
1000 genomesrs121908873
hgdprs121908873
ensemblrs121908873
gopubmedrs121908873
geneviewrs121908873
scholarrs121908873
googlers121908873
pharmgkbrs121908873
gwascentralrs121908873
openSNPrs121908873
23andMers121908873
23andMe allrs121908873
SNP Nexus

SNPshotrs121908873
SNPdbers121908873
MSV3drs121908873
GWAS Ctlgrs121908873
Merged fromRs121908878
Max Magnitude0
OMIM603372
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121908873(A,T;A,T)
Alt rs121908873(A,T;A,T)
Reference rs121908873(G;G)
Significance Pathogenic
Disease Hyperthyroidism Thyroid adenoma
Variation info
Gene LOC101928431 TSHR
CLNDBN Hyperthyroidism, nonautoimmune Thyroid adenoma, hyperfunctioning
Reversed 0
HGVS NC_000014.8:g.81606172G>A; NC_000014.8:g.81606172G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006823.2, RCV000006816.4,