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rs121908885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908885(C;C)
Make rs121908885(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position81143458
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs121908885
dbSNP (classic)rs121908885
ClinGenrs121908885
ebirs121908885
HLIrs121908885
Exacrs121908885
Gnomadrs121908885
Varsomers121908885
LitVarrs121908885
Maprs121908885
PheGenIrs121908885
Biobankrs121908885
1000 genomesrs121908885
hgdprs121908885
ensemblrs121908885
geneviewrs121908885
scholarrs121908885
googlers121908885
pharmgkbrs121908885
gwascentralrs121908885
openSNPrs121908885
23andMers121908885
SNPshotrs121908885
SNPdbers121908885
MSV3drs121908885
GWAS Ctlgrs121908885
Max Magnitude0
OMIM603372
Desc
Variant0030
Relatedalso
ClinVar
Risk rs121908885(C;C)
Alt rs121908885(C;C)
Reference Rs121908885(T;T)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene LOC101928431 TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81609802T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006830.3,