Rs121908859

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Orientationplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121908859(A;G)
Make rs121908859(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143914
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908859
Exacrs121908859
PheGenIrs121908859
nextbiors121908859
hapmaprs121908859
1000 genomesrs121908859
hgdprs121908859
ensemblrs121908859
gopubmedrs121908859
geneviewrs121908859
scholarrs121908859
googlers121908859
pharmgkbrs121908859
gwascentralrs121908859
openSNPrs121908859
23andMers121908859
23andMe allrs121908859
SNP Nexus

SNPshotrs121908859
SNPdbers121908859
MSV3drs121908859
OMIM603372
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908859(G;G)
Alt rs121908859(G;G)
Reference rs121908859(A;A)
Significance Other
Disease Thyroid adenoma
Variation info
Gene TSHR
CLNDBN Thyroid adenoma, hyperfunctioning, somatic
Reversed 0
HGVS NC_000014.8:g.81610258A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006800.1,