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rs283566

From SNPedia

Orientationminus
Stabilizedminus
Make rs283566(C;C)
Make rs283566(C;G)
Make rs283566(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position51091008
is asnp
is mentioned by
dbSNPrs283566
ebirs283566
HLIrs283566
Exacrs283566
Varsomers283566
Maprs283566
PheGenIrs283566
hapmaprs283566
1000 genomesrs283566
hgdprs283566
ensemblrs283566
gopubmedrs283566
geneviewrs283566
scholarrs283566
googlers283566
pharmgkbrs283566
gwascentralrs283566
openSNPrs283566
23andMers283566
23andMe allrs283566
SNP Nexus

SNPshotrs283566
SNPdbers283566
MSV3drs283566
GWAS Ctlgrs283566
GMAF0.388
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19389651OA-icon.png]
Trait Electrocardiographic conduction measures
Title Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae
Risk Allele
P-val 0.000009
Odds Ratio NR NR


GET Evidence
rs283566
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.555556
summary