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Rs121908882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908882(C;T)
Make rs121908882(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81142986
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908882
ebirs121908882
Exacrs121908882
PheGenIrs121908882
nextbiors121908882
hapmaprs121908882
1000 genomesrs121908882
hgdprs121908882
ensemblrs121908882
gopubmedrs121908882
geneviewrs121908882
scholarrs121908882
googlers121908882
pharmgkbrs121908882
gwascentralrs121908882
openSNPrs121908882
23andMers121908882
23andMe allrs121908882
SNP Nexus

SNPshotrs121908882
SNPdbers121908882
MSV3drs121908882
GWAS Ctlgrs121908882
Max Magnitude0
OMIM603372
Desc
Variant0027
Relatedalso
ClinVar
Risk rs121908882(T;T)
Alt rs121908882(T;T)
Reference rs121908882(C;C)
Significance Pathogenic
Disease Hypothyroidism not specified
Variation info
Gene LOC101928431 TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1 not specified
Reversed 0
HGVS NC_000014.9:g.81142986C>T
CLNSRC ClinVar OMIM Allelic Variant
CLNACC RCV000006827.1, RCV000122250.1,