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rs13418717

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs13418717(A;A)
Make rs13418717(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position126905321
is asnp
is mentioned by
dbSNPrs13418717
ebirs13418717
HLIrs13418717
Exacrs13418717
Varsomers13418717
Maprs13418717
PheGenIrs13418717
hapmaprs13418717
1000 genomesrs13418717
hgdprs13418717
ensemblrs13418717
gopubmedrs13418717
geneviewrs13418717
scholarrs13418717
googlers13418717
pharmgkbrs13418717
gwascentralrs13418717
openSNPrs13418717
23andMers13418717
23andMe allrs13418717
SNP Nexus

SNPshotrs13418717
SNPdbers13418717
MSV3drs13418717
GWAS Ctlgrs13418717
GMAF0.1331
Max Magnitude0
? (A;A) (A;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 0.000003
Odds Ratio 1.46 [0.97-2.20]