Rs121908881

From SNPedia
Jump to: navigation, search

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908881(C;T)
Make rs121908881(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143488
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908881
Exacrs121908881
PheGenIrs121908881
nextbiors121908881
hapmaprs121908881
1000 genomesrs121908881
hgdprs121908881
ensemblrs121908881
gopubmedrs121908881
geneviewrs121908881
scholarrs121908881
googlers121908881
pharmgkbrs121908881
gwascentralrs121908881
openSNPrs121908881
23andMers121908881
23andMe allrs121908881
SNP Nexus

SNPshotrs121908881
SNPdbers121908881
MSV3drs121908881
OMIM603372
Desc
Variant0026
Relatedalso
ClinVar
Risk rs121908881(T;T)
Alt rs121908881(T;T)
Reference rs121908881(C;C)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81609832C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006826.1,