Rs121908884

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908884(C;C)
Make rs121908884(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143856
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908884
Exacrs121908884
PheGenIrs121908884
nextbiors121908884
hapmaprs121908884
1000 genomesrs121908884
hgdprs121908884
ensemblrs121908884
gopubmedrs121908884
geneviewrs121908884
scholarrs121908884
googlers121908884
pharmgkbrs121908884
gwascentralrs121908884
openSNPrs121908884
23andMers121908884
23andMe allrs121908884
SNP Nexus

SNPshotrs121908884
SNPdbers121908884
MSV3drs121908884
Max Magnitude0
OMIM603372
Desc
Variant0029
Relatedalso
ClinVar
Risk rs121908884(C;C)
Alt rs121908884(C;C)
Reference rs121908884(T;T)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81610200T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006829.1,