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rs2562456

From SNPedia

Orientationminus
Stabilizedminus
Make rs2562456(A;A)
Make rs2562456(A;G)
Make rs2562456(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position21483408
GeneFTLP13
is asnp
is mentioned by
dbSNPrs2562456
ebirs2562456
HLIrs2562456
Exacrs2562456
Varsomers2562456
Maprs2562456
PheGenIrs2562456
hapmaprs2562456
1000 genomesrs2562456
hgdprs2562456
ensemblrs2562456
gopubmedrs2562456
geneviewrs2562456
scholarrs2562456
googlers2562456
pharmgkbrs2562456
gwascentralrs2562456
openSNPrs2562456
23andMers2562456
23andMe allrs2562456
SNP Nexus

SNPshotrs2562456
SNPdbers2562456
MSV3drs2562456
GWAS Ctlgrs2562456
GMAF0.2355
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19207018OA-icon.png]
Trait Pain
Title Genome-wide association study of acute post-surgical pain in humans
Risk Allele
P-val 2E-10
Odds Ratio NR NR



GET Evidence
rs2562456
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.776786
summary