Rs121908875

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908875(A;A)
Make rs121908875(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position81144073
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908875
Exacrs121908875
PheGenIrs121908875
nextbiors121908875
hapmaprs121908875
1000 genomesrs121908875
hgdprs121908875
ensemblrs121908875
gopubmedrs121908875
geneviewrs121908875
scholarrs121908875
googlers121908875
pharmgkbrs121908875
gwascentralrs121908875
openSNPrs121908875
23andMers121908875
23andMe allrs121908875
SNP Nexus

SNPshotrs121908875
SNPdbers121908875
MSV3drs121908875
OMIM603372
Desc
Variant0020
Relatedalso
ClinVar
Risk rs121908875(A;A)
Alt rs121908875(A;A)
Reference rs121908875(G;G)
Significance Pathogenic
Disease Hyperthyroidism
Variation info
Gene TSHR
CLNDBN Hyperthyroidism, nonautoimmune
Reversed 0
HGVS NC_000014.8:g.81610417G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006819.1,