rs116909374

plus

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

Make rs116909374(C;T)

Make rs116909374(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

36269155

is a	snp
is	mentioned by
dbSNP	rs116909374
dbSNP (classic)	rs116909374
ClinGen	rs116909374
ebi	rs116909374
HLI	rs116909374
Exac	rs116909374
Gnomad	rs116909374
Varsome	rs116909374
LitVar	rs116909374
Map	rs116909374
PheGenI	rs116909374
Biobank	rs116909374
1000 genomes	rs116909374
hgdp	rs116909374
ensembl	rs116909374
geneview	rs116909374
scholar	rs116909374
google	rs116909374
pharmgkb	rs116909374
gwascentral	rs116909374
openSNP	rs116909374
23andMe	rs116909374
SNPshot	rs116909374
SNPdbe	rs116909374
MSV3d	rs116909374
GWAS Ctlg	rs116909374

GMAF

0.01928

Max Magnitude

0

GWAS snp
PMID	[PMID 22267200 ]
Trait
Title	Discovery of common variants associated with low TSH levels and thyroid cancer risk.
Risk Allele	T
P-val	5E-11
Odds Ratio	2.0900 None

[PMID 23659773 ] Cumulative Risk Impact of Five Genetic Variants Associated With Papillary Thyroid Carcinoma

[PMID 23847140] Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population

[PMID 24591304 ] Significant SNPs have limited prediction ability for thyroid cancer

[PMID 26490305] Association Between GWAS-derived rs966423 Genetic Variant and Overall Mortality in Patients with Differentiated Thyroid Cancer

[PMID 31681970] Clinical implications of GWAS variants associated with differentiated thyroid cancer.