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rs121908862

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908862(A;A)
Make rs121908862(A;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81092563
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs121908862
ebirs121908862
HLIrs121908862
Exacrs121908862
Varsomers121908862
Maprs121908862
PheGenIrs121908862
hapmaprs121908862
1000 genomesrs121908862
hgdprs121908862
ensemblrs121908862
gopubmedrs121908862
geneviewrs121908862
scholarrs121908862
googlers121908862
pharmgkbrs121908862
gwascentralrs121908862
openSNPrs121908862
23andMers121908862
23andMe allrs121908862
SNP Nexus

SNPshotrs121908862
SNPdbers121908862
MSV3drs121908862
GWAS Ctlgrs121908862
Max Magnitude0
OMIM603372
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908862(A;A)
Alt rs121908862(A;A)
Reference rs121908862(T;T)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene LOC101928462 TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81558907T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006804.3,