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rs12826786

From SNPedia

Orientationplus
Make rs12826786(C;C)
Make rs12826786(C;T)
Make rs12826786(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position53961717
is asnp
is mentioned by
dbSNPrs12826786
ebirs12826786
HLIrs12826786
Exacrs12826786
Varsomers12826786
Maprs12826786
PheGenIrs12826786
hapmaprs12826786
1000 genomesrs12826786
hgdprs12826786
ensemblrs12826786
gopubmedrs12826786
geneviewrs12826786
scholarrs12826786
googlers12826786
pharmgkbrs12826786
gwascentralrs12826786
openSNPrs12826786
23andMers12826786
23andMe allrs12826786
SNP Nexus

SNPshotrs12826786
SNPdbers12826786
MSV3drs12826786
GWAS Ctlgrs12826786
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26577852] A functional HOTAIR rs12826786 C>T polymorphism is associated with breast cancer susceptibility and poor clinicopathological characteristics in a Turkish population: a hospital-based case-control study