Rs121908860

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Orientationplus
Geno Mag Summary
(GC;GC) 0 common in complete genomics
Make rs121908860(AT;AT)
Make rs121908860(AT;GC)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143925
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908860
Exacrs121908860
PheGenIrs121908860
nextbiors121908860
hapmaprs121908860
1000 genomesrs121908860
hgdprs121908860
ensemblrs121908860
gopubmedrs121908860
geneviewrs121908860
scholarrs121908860
googlers121908860
pharmgkbrs121908860
gwascentralrs121908860
openSNPrs121908860
23andMers121908860
23andMe allrs121908860
SNP Nexus

SNPshotrs121908860
SNPdbers121908860
MSV3drs121908860
Max Magnitude0
OMIM603372
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908860(AT;AT)
Alt rs121908860(AT;AT)
Reference rs121908860(GC;GC)
Significance Other
Disease Thyroid adenoma
Variation info
Gene TSHR
CLNDBN Thyroid adenoma, hyperfunctioning, somatic
Reversed 0
HGVS NC_000014.8:g.81610269_81610270delGCinsAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006801.1,