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rs1871152

From SNPedia

Orientationminus
Make rs1871152(C;C)
Make rs1871152(C;T)
Make rs1871152(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position28226893
GeneCCDC91
is asnp
is mentioned by
dbSNPrs1871152
ebirs1871152
HLIrs1871152
Exacrs1871152
Varsomers1871152
Maprs1871152
PheGenIrs1871152
hapmaprs1871152
1000 genomesrs1871152
hgdprs1871152
ensemblrs1871152
gopubmedrs1871152
geneviewrs1871152
scholarrs1871152
googlers1871152
pharmgkbrs1871152
gwascentralrs1871152
openSNPrs1871152
23andMers1871152
23andMe allrs1871152
SNP Nexus

SNPshotrs1871152
SNPdbers1871152
MSV3drs1871152
GWAS Ctlgrs1871152
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.