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rs6995588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6995588(C;T)
Make rs6995588(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position60091338
is asnp
is mentioned by
dbSNPrs6995588
ebirs6995588
HLIrs6995588
Exacrs6995588
Varsomers6995588
Maprs6995588
PheGenIrs6995588
hapmaprs6995588
1000 genomesrs6995588
hgdprs6995588
ensemblrs6995588
gopubmedrs6995588
geneviewrs6995588
scholarrs6995588
googlers6995588
pharmgkbrs6995588
gwascentralrs6995588
openSNPrs6995588
23andMers6995588
23andMe allrs6995588
SNP Nexus

SNPshotrs6995588
SNPdbers6995588
MSV3drs6995588
GWAS Ctlgrs6995588
GMAF0.1084
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21348951OA-icon.png]
Trait
Title Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality
Risk Allele
P-val 0.000002
Odds Ratio None None