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rs17018765

From SNPedia

Orientationplus
Stabilizedplus
Make rs17018765(A;A)
Make rs17018765(A;G)
Make rs17018765(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position91115372
is asnp
is mentioned by
dbSNPrs17018765
dbSNP (classic)rs17018765
ClinGenrs17018765
ebirs17018765
HLIrs17018765
Exacrs17018765
Gnomadrs17018765
Varsomers17018765
LitVarrs17018765
Maprs17018765
PheGenIrs17018765
Biobankrs17018765
1000 genomesrs17018765
hgdprs17018765
ensemblrs17018765
geneviewrs17018765
scholarrs17018765
googlers17018765
pharmgkbrs17018765
gwascentralrs17018765
openSNPrs17018765
23andMers17018765
SNPshotrs17018765
SNPdbers17018765
MSV3drs17018765
GWAS Ctlgrs17018765
GMAF0.07622
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 21637745OA-icon.png] Polymorphisms in stromal genes and susceptibility to serous epithelial ovarian cancer: a report from the ovarian cancer association consortium


[PMID 19036156OA-icon.png] Genetic variation in stromal proteins decorin and lumican with breast cancer: investigations in two case-control studies.