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rs876657394

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657394(A;A)
Make rs876657394(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position40089399
GeneTHRA
is asnp
is mentioned by
dbSNPrs876657394
ebirs876657394
HLIrs876657394
Exacrs876657394
Varsomers876657394
Maprs876657394
PheGenIrs876657394
hapmaprs876657394
1000 genomesrs876657394
hgdprs876657394
ensemblrs876657394
gopubmedrs876657394
geneviewrs876657394
scholarrs876657394
googlers876657394
pharmgkbrs876657394
gwascentralrs876657394
openSNPrs876657394
23andMers876657394
23andMe allrs876657394
SNP Nexus

SNPshotrs876657394
SNPdbers876657394
MSV3drs876657394
GWAS Ctlgrs876657394
Max Magnitude0
ClinVar
Risk rs876657394(A;A)
Alt rs876657394(A;A)
Reference rs876657394(C;C)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene THRA
CLNDBN Hypothyroidism, congenital, nongoitrous, 6
Reversed 0
HGVS NC_000017.10:g.38245652C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172853.2,