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rs40457

From SNPedia

Orientationplus
Stabilizedplus
Make rs40457(A;A)
Make rs40457(A;G)
Make rs40457(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position89811459
is asnp
is mentioned by
dbSNPrs40457
ebirs40457
HLIrs40457
Exacrs40457
Varsomers40457
Maprs40457
PheGenIrs40457
hapmaprs40457
1000 genomesrs40457
hgdprs40457
ensemblrs40457
gopubmedrs40457
geneviewrs40457
scholarrs40457
googlers40457
pharmgkbrs40457
gwascentralrs40457
openSNPrs40457
23andMers40457
23andMe allrs40457
SNP Nexus

SNPshotrs40457
SNPdbers40457
MSV3drs40457
GWAS Ctlgrs40457
GMAF0.4793
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20018961]
Trait Leprosy
Title Genomewide Association Study of Leprosy
Risk Allele A
P-val 1E-12
Odds Ratio 1.30 [1.20-1.39]


GET Evidence
rs40457
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.546875
summary