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

rs5916687

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs5916687(A;A)
Make rs5916687(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position4678097
is asnp
is mentioned by
dbSNPrs5916687
ebirs5916687
HLIrs5916687
Exacrs5916687
Varsomers5916687
Maprs5916687
PheGenIrs5916687
hapmaprs5916687
1000 genomesrs5916687
hgdprs5916687
ensemblrs5916687
gopubmedrs5916687
geneviewrs5916687
scholarrs5916687
googlers5916687
pharmgkbrs5916687
gwascentralrs5916687
openSNPrs5916687
23andMers5916687
23andMe allrs5916687
SNP Nexus

SNPshotrs5916687
SNPdbers5916687
MSV3drs5916687
GWAS Ctlgrs5916687
GMAF0.1288
Max Magnitude0
? (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 1.22 [NR]


GET Evidence
rs5916687
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.188889
summary