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rs11169571

From SNPedia

Orientationplus
Stabilizedplus
Make rs11169571(C;C)
Make rs11169571(C;T)
Make rs11169571(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position50819982
GeneATF1
is asnp
is mentioned by
dbSNPrs11169571
ebirs11169571
HLIrs11169571
Exacrs11169571
Varsomers11169571
Maprs11169571
PheGenIrs11169571
hapmaprs11169571
1000 genomesrs11169571
hgdprs11169571
ensemblrs11169571
gopubmedrs11169571
geneviewrs11169571
scholarrs11169571
googlers11169571
pharmgkbrs11169571
gwascentralrs11169571
openSNPrs11169571
23andMers11169571
23andMe allrs11169571
SNP Nexus

SNPshotrs11169571
SNPdbers11169571
MSV3drs11169571
GWAS Ctlgrs11169571
GMAF0.3421
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19950226] SNPs in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high risk women


[PMID 26149214] The human ATF1 rs11169571 polymorphism increases essential hypertension risk through modifying miRNA binding