Rs121908867

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908867(C;T)
Make rs121908867(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143028
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908867
Exacrs121908867
PheGenIrs121908867
nextbiors121908867
hapmaprs121908867
1000 genomesrs121908867
hgdprs121908867
ensemblrs121908867
gopubmedrs121908867
geneviewrs121908867
scholarrs121908867
googlers121908867
pharmgkbrs121908867
gwascentralrs121908867
openSNPrs121908867
23andMers121908867
23andMe allrs121908867
SNP Nexus

SNPshotrs121908867
SNPdbers121908867
MSV3drs121908867
OMIM603372
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121908867(T;T)
Alt rs121908867(T;T)
Reference rs121908867(C;C)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81609372C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006810.1,