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rs2461751

From SNPedia

Orientationminus
Stabilizedminus
Make rs2461751(C;C)
Make rs2461751(C;T)
Make rs2461751(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position175424591
is asnp
is mentioned by
dbSNPrs2461751
ebirs2461751
HLIrs2461751
Exacrs2461751
Varsomers2461751
Maprs2461751
PheGenIrs2461751
hapmaprs2461751
1000 genomesrs2461751
hgdprs2461751
ensemblrs2461751
gopubmedrs2461751
geneviewrs2461751
scholarrs2461751
googlers2461751
pharmgkbrs2461751
gwascentralrs2461751
openSNPrs2461751
23andMers2461751
23andMe allrs2461751
SNP Nexus

SNPshotrs2461751
SNPdbers2461751
MSV3drs2461751
GWAS Ctlgrs2461751
GMAF0.298
Max Magnitude
? (C;C) (C;T) (T;T) 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 G
P-val 0.000008
Odds Ratio 4.54 [2.58-6.50] ms increase


GET Evidence
rs2461751
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.304688
summary