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rs7698598

From SNPedia

Orientationplus
Stabilizedplus
Make rs7698598(A;A)
Make rs7698598(A;G)
Make rs7698598(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position119030492
GeneSYNPO2
is asnp
is mentioned by
dbSNPrs7698598
ebirs7698598
HLIrs7698598
Exacrs7698598
Varsomers7698598
Maprs7698598
PheGenIrs7698598
hapmaprs7698598
1000 genomesrs7698598
hgdprs7698598
ensemblrs7698598
gopubmedrs7698598
geneviewrs7698598
scholarrs7698598
googlers7698598
pharmgkbrs7698598
gwascentralrs7698598
openSNPrs7698598
23andMers7698598
23andMe allrs7698598
SNP Nexus

SNPshotrs7698598
SNPdbers7698598
MSV3drs7698598
GWAS Ctlgrs7698598
Max Magnitude
GWAS snp
PMID [PMID 24529757]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val 2E-6
Odds Ratio NR NR