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rs11705932

From SNPedia

Orientationplus
Make rs11705932(C;C)
Make rs11705932(C;T)
Make rs11705932(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position142100008
GeneTFDP2
is asnp
is mentioned by
dbSNPrs11705932
ebirs11705932
HLIrs11705932
Exacrs11705932
Varsomers11705932
Maprs11705932
PheGenIrs11705932
hapmaprs11705932
1000 genomesrs11705932
hgdprs11705932
ensemblrs11705932
gopubmedrs11705932
geneviewrs11705932
scholarrs11705932
googlers11705932
pharmgkbrs11705932
gwascentralrs11705932
openSNPrs11705932
23andMers11705932
23andMe allrs11705932
SNP Nexus

SNPshotrs11705932
SNPdbers11705932
MSV3drs11705932
GWAS Ctlgrs11705932
Max Magnitude
? (C;C) (C;T) (T;T) 28
A multi-stage GWAS study of 6,000+ patients with testicular cancer found this SNP (and 3 others) to be associated with slightly higher risk (OR 1.18 for risk allele C; CI: 1.09–1.28, p=1.5x10e−9) for the disease. See also the testicular cancer page for the discussion of this and the 24 other SNPs used in a polygenic risk score.[PMID 26503584OA-icon.png]