Have questions? Visit https://www.reddit.com/r/SNPedia

rs2405657

From SNPedia

Orientationplus
Stabilizedplus
Make rs2405657(A;A)
Make rs2405657(A;G)
Make rs2405657(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position97811564
is asnp
is mentioned by
dbSNPrs2405657
ebirs2405657
HLIrs2405657
Exacrs2405657
Varsomers2405657
Maprs2405657
PheGenIrs2405657
hapmaprs2405657
1000 genomesrs2405657
hgdprs2405657
ensemblrs2405657
gopubmedrs2405657
geneviewrs2405657
scholarrs2405657
googlers2405657
pharmgkbrs2405657
gwascentralrs2405657
openSNPrs2405657
23andMers2405657
23andMe allrs2405657
SNP Nexus

SNPshotrs2405657
SNPdbers2405657
MSV3drs2405657
GWAS Ctlgrs2405657
GMAF0.4096
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19734901]
Trait Amyotrophic lateral sclerosis
Title Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
Risk Allele
P-val 0.000003
Odds Ratio 1.19 [NR]


GET Evidence
rs2405657
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.65873
summary