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rs10961534

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10961534(A;G)
Make rs10961534(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position14470835
is asnp
is mentioned by
dbSNPrs10961534
ebirs10961534
HLIrs10961534
Exacrs10961534
Varsomers10961534
Maprs10961534
PheGenIrs10961534
hapmaprs10961534
1000 genomesrs10961534
hgdprs10961534
ensemblrs10961534
gopubmedrs10961534
geneviewrs10961534
scholarrs10961534
googlers10961534
pharmgkbrs10961534
gwascentralrs10961534
openSNPrs10961534
23andMers10961534
23andMe allrs10961534
SNP Nexus

SNPshotrs10961534
SNPdbers10961534
MSV3drs10961534
GWAS Ctlgrs10961534
GMAF0.1878
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22493691OA-icon.png]
Trait
Title Novel associations for hypothyroidism include known autoimmune risk loci.
Risk Allele G
P-val 0.000007
Odds Ratio 1.1930 None