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rs11118620

From SNPedia

Orientationplus
Stabilizedplus
Make rs11118620(C;C)
Make rs11118620(C;T)
Make rs11118620(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position220855166
GeneHLX-AS1
is asnp
is mentioned by
dbSNPrs11118620
ebirs11118620
HLIrs11118620
Exacrs11118620
Varsomers11118620
Maprs11118620
PheGenIrs11118620
hapmaprs11118620
1000 genomesrs11118620
hgdprs11118620
ensemblrs11118620
gopubmedrs11118620
geneviewrs11118620
scholarrs11118620
googlers11118620
pharmgkbrs11118620
gwascentralrs11118620
openSNPrs11118620
23andMers11118620
23andMe allrs11118620
SNP Nexus

SNPshotrs11118620
SNPdbers11118620
MSV3drs11118620
GWAS Ctlgrs11118620
GMAF0.3246
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20445134OA-icon.png]
Trait Heart failure
Title The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium
Risk Allele
P-val 0.000007
Odds Ratio 1.15 [0.98-1.35]