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rs11049453

From SNPedia

Orientationplus
Make rs11049453(A;A)
Make rs11049453(A;G)
Make rs11049453(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position28202996
GeneCCDC91
is asnp
is mentioned by
dbSNPrs11049453
ebirs11049453
HLIrs11049453
Exacrs11049453
Varsomers11049453
Maprs11049453
PheGenIrs11049453
hapmaprs11049453
1000 genomesrs11049453
hgdprs11049453
ensemblrs11049453
gopubmedrs11049453
geneviewrs11049453
scholarrs11049453
googlers11049453
pharmgkbrs11049453
gwascentralrs11049453
openSNPrs11049453
23andMers11049453
23andMe allrs11049453
SNP Nexus

SNPshotrs11049453
SNPdbers11049453
MSV3drs11049453
GWAS Ctlgrs11049453
Max Magnitude

[PMID 27459855] Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.