rs10961534

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs10961534(A;G)

Make rs10961534(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

14470835

is a	snp
is	mentioned by
dbSNP	rs10961534
dbSNP (classic)	rs10961534
ClinGen	rs10961534
ebi	rs10961534
HLI	rs10961534
Exac	rs10961534
Gnomad	rs10961534
Varsome	rs10961534
LitVar	rs10961534
Map	rs10961534
PheGenI	rs10961534
Biobank	rs10961534
1000 genomes	rs10961534
hgdp	rs10961534
ensembl	rs10961534
geneview	rs10961534
scholar	rs10961534
google	rs10961534
pharmgkb	rs10961534
gwascentral	rs10961534
openSNP	rs10961534
23andMe	rs10961534
SNPshot	rs10961534
SNPdbe	rs10961534
MSV3d	rs10961534
GWAS Ctlg	rs10961534

GMAF

0.1878

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 22493691]
Trait
Title	Novel associations for hypothyroidism include known autoimmune risk loci.
Risk Allele	G
P-val	0.000007
Odds Ratio	1.1930 None