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

rs17162257

From SNPedia

Orientationplus
Stabilizedplus
Make rs17162257(G;G)
Make rs17162257(G;T)
Make rs17162257(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position26602511
is asnp
is mentioned by
dbSNPrs17162257
ebirs17162257
HLIrs17162257
Exacrs17162257
Varsomers17162257
Maprs17162257
PheGenIrs17162257
hapmaprs17162257
1000 genomesrs17162257
hgdprs17162257
ensemblrs17162257
gopubmedrs17162257
geneviewrs17162257
scholarrs17162257
googlers17162257
pharmgkbrs17162257
gwascentralrs17162257
openSNPrs17162257
23andMers17162257
23andMe allrs17162257
SNP Nexus

SNPshotrs17162257
SNPdbers17162257
MSV3drs17162257
GWAS Ctlgrs17162257
Max Magnitude
? (G;G) (G;T) (T;T) 28
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 1E-6
Odds Ratio NR NR