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rs876657395

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657395(A;A)
Make rs876657395(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position40089430
GeneTHRA
is asnp
is mentioned by
dbSNPrs876657395
ebirs876657395
HLIrs876657395
Exacrs876657395
Varsomers876657395
Maprs876657395
PheGenIrs876657395
hapmaprs876657395
1000 genomesrs876657395
hgdprs876657395
ensemblrs876657395
gopubmedrs876657395
geneviewrs876657395
scholarrs876657395
googlers876657395
pharmgkbrs876657395
gwascentralrs876657395
openSNPrs876657395
23andMers876657395
23andMe allrs876657395
SNP Nexus

SNPshotrs876657395
SNPdbers876657395
MSV3drs876657395
GWAS Ctlgrs876657395
Max Magnitude0
ClinVar
Risk rs876657395(A;A)
Alt rs876657395(A;A)
Reference rs876657395(G;G)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene THRA
CLNDBN Hypothyroidism, congenital, nongoitrous, 6
Reversed 0
HGVS NC_000017.10:g.38245683G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172854.2,