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rs3790672

From SNPedia

Orientationplus
Stabilizedplus
Make rs3790672(C;C)
Make rs3790672(C;T)
Make rs3790672(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position165904155
GeneUCK2
is asnp
is mentioned by
dbSNPrs3790672
dbSNP (classic)rs3790672
ClinGenrs3790672
ebirs3790672
HLIrs3790672
Exacrs3790672
Gnomadrs3790672
Varsomers3790672
LitVarrs3790672
Maprs3790672
PheGenIrs3790672
Biobankrs3790672
1000 genomesrs3790672
hgdprs3790672
ensemblrs3790672
geneviewrs3790672
scholarrs3790672
googlers3790672
pharmgkbrs3790672
gwascentralrs3790672
openSNPrs3790672
23andMers3790672
SNPshotrs3790672
SNPdbers3790672
MSV3drs3790672
GWAS Ctlgrs3790672
GMAF0.3154
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23666240OA-icon.png]
Trait Testicular germ cell tumor
Title Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.
Risk Allele C
P-val 2E-8
Odds Ratio 1.20 [1.09-1.33]