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rs16943468

From SNPedia

Orientationplus
Stabilizedplus
Make rs16943468(C;C)
Make rs16943468(C;T)
Make rs16943468(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position59367748
GeneYPEL2
is asnp
is mentioned by
dbSNPrs16943468
ebirs16943468
HLIrs16943468
Exacrs16943468
Varsomers16943468
Maprs16943468
PheGenIrs16943468
hapmaprs16943468
1000 genomesrs16943468
hgdprs16943468
ensemblrs16943468
gopubmedrs16943468
geneviewrs16943468
scholarrs16943468
googlers16943468
pharmgkbrs16943468
gwascentralrs16943468
openSNPrs16943468
23andMers16943468
23andMe allrs16943468
SNP Nexus

SNPshotrs16943468
SNPdbers16943468
MSV3drs16943468
GWAS Ctlgrs16943468
GMAF0.1309
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19454617OA-icon.png] Genetic variation in the chromosome 17q23 amplicon and breast cancer risk