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rs121908861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908861(C;C)
Make rs121908861(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143949
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908861
ebirs121908861
HLIrs121908861
Exacrs121908861
Varsomers121908861
Maprs121908861
PheGenIrs121908861
hapmaprs121908861
1000 genomesrs121908861
hgdprs121908861
ensemblrs121908861
gopubmedrs121908861
geneviewrs121908861
scholarrs121908861
googlers121908861
pharmgkbrs121908861
gwascentralrs121908861
openSNPrs121908861
23andMers121908861
23andMe allrs121908861
SNP Nexus

SNPshotrs121908861
SNPdbers121908861
MSV3drs121908861
GWAS Ctlgrs121908861
Max Magnitude0
OMIM603372
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908861(C;C)
Alt rs121908861(C;C)
Reference rs121908861(T;T)
Significance Pathogenic
Disease Hyperthyroidism Thyroid adenoma
Variation info
Gene LOC101928431 TSHR
CLNDBN Hyperthyroidism, nonautoimmune Thyroid adenoma, hyperfunctioning
Reversed 0
HGVS NC_000014.8:g.81610293T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006802.2, RCV000006803.4,