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rs12826786

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (old)rs12826786
ClinGenrs12826786
ebirs12826786
HLIrs12826786
Exacrs12826786
Gnomadrs12826786
Varsomers12826786
Maprs12826786
PheGenIrs12826786
Biobankrs12826786
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

[PMID 28083786] Effects of the functional HOTAIR rs920778 and rs12826786 genetic variants in glioma susceptibility and patient prognosis.

[PMID 28259691] HOTAIR genetic variants are associated with prostate cancer and benign prostate hyperplasia in an Iranian population.

[PMID 28342055] The analysis of lncRNA HOTAIR rs12826786 C>T polymorphism and gastric cancer susceptibility in a Turkish population: lack of any association in a hospital-based case-control study.