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rs13074711

From SNPedia

Orientationplus
Make rs13074711(C;C)
Make rs13074711(C;T)
Make rs13074711(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position172550013
is asnp
is mentioned by
dbSNPrs13074711
ebirs13074711
HLIrs13074711
Exacrs13074711
Varsomers13074711
Maprs13074711
PheGenIrs13074711
hapmaprs13074711
1000 genomesrs13074711
hgdprs13074711
ensemblrs13074711
gopubmedrs13074711
geneviewrs13074711
scholarrs13074711
googlers13074711
pharmgkbrs13074711
gwascentralrs13074711
openSNPrs13074711
23andMers13074711
23andMe allrs13074711
SNP Nexus

SNPshotrs13074711
SNPdbers13074711
MSV3drs13074711
GWAS Ctlgrs13074711
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 27594435] Genome-wide Association Studies in Women of African Ancestry Identified 3q26.21 as a Novel Susceptibility Locus for Estrogen Receptor Negative Breast Cancer.