Rs121908885

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908885(C;C)
Make rs121908885(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143458
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908885
Exacrs121908885
PheGenIrs121908885
nextbiors121908885
hapmaprs121908885
1000 genomesrs121908885
hgdprs121908885
ensemblrs121908885
gopubmedrs121908885
geneviewrs121908885
scholarrs121908885
googlers121908885
pharmgkbrs121908885
gwascentralrs121908885
openSNPrs121908885
23andMers121908885
23andMe allrs121908885
SNP Nexus

SNPshotrs121908885
SNPdbers121908885
MSV3drs121908885
Max Magnitude0
OMIM603372
Desc
Variant0030
Relatedalso
ClinVar
Risk rs121908885(C;C)
Alt rs121908885(C;C)
Reference rs121908885(T;T)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81609802T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006830.1,