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rs876657396

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657396(C;G)
Make rs876657396(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position40089416
GeneTHRA
is asnp
is mentioned by
dbSNPrs876657396
ebirs876657396
HLIrs876657396
Exacrs876657396
Varsomers876657396
Maprs876657396
PheGenIrs876657396
hapmaprs876657396
1000 genomesrs876657396
hgdprs876657396
ensemblrs876657396
gopubmedrs876657396
geneviewrs876657396
scholarrs876657396
googlers876657396
pharmgkbrs876657396
gwascentralrs876657396
openSNPrs876657396
23andMers876657396
23andMe allrs876657396
SNP Nexus

SNPshotrs876657396
SNPdbers876657396
MSV3drs876657396
GWAS Ctlgrs876657396
Max Magnitude0
ClinVar
Risk rs876657396(G;G)
Alt rs876657396(G;G)
Reference rs876657396(C;C)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene THRA
CLNDBN Hypothyroidism, congenital, nongoitrous, 6
Reversed 0
HGVS NC_000017.10:g.38245669C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000172855.2,