Rs121908871

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908871(G;G)
Make rs121908871(G;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143228
GeneLOC101928431, TSHR
is asnp
is mentioned by
dbSNPrs121908871
PheGenIrs121908871
nextbiors121908871
hapmaprs121908871
1000 genomesrs121908871
hgdprs121908871
ensemblrs121908871
gopubmedrs121908871
geneviewrs121908871
scholarrs121908871
googlers121908871
pharmgkbrs121908871
gwascentralrs121908871
openSNPrs121908871
23andMers121908871
23andMe allrs121908871
SNP Nexus

SNPshotrs121908871
SNPdbers121908871
MSV3drs121908871
Max Magnitude0
OMIM603372
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121908871(G;G)
Alt rs121908871(G;G)
Reference rs121908871(T;T)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81609572T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006814.1,