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rs7580332

From SNPedia

Orientationplus
Stabilizedplus
Make rs7580332(A;A)
Make rs7580332(A;G)
Make rs7580332(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position18359378
is asnp
is mentioned by
dbSNPrs7580332
ebirs7580332
HLIrs7580332
Exacrs7580332
Varsomers7580332
Maprs7580332
PheGenIrs7580332
hapmaprs7580332
1000 genomesrs7580332
hgdprs7580332
ensemblrs7580332
gopubmedrs7580332
geneviewrs7580332
scholarrs7580332
googlers7580332
pharmgkbrs7580332
gwascentralrs7580332
openSNPrs7580332
23andMers7580332
23andMe allrs7580332
SNP Nexus

SNPshotrs7580332
SNPdbers7580332
MSV3drs7580332
GWAS Ctlgrs7580332
GMAF0.3512
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18084291]
Trait Amyotrophic lateral sclerosis
Title Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis
Risk Allele
P-val 0.0000090000000000000002
Odds Ratio 1.22 [1.09-1.35]


GET Evidence
rs7580332
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.265625
summary