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

rs17603886

From SNPedia

Orientationplus
Stabilizedplus
Make rs17603886(C;C)
Make rs17603886(C;T)
Make rs17603886(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position10443042
GeneATP2B2
is asnp
is mentioned by
dbSNPrs17603886
ebirs17603886
HLIrs17603886
Exacrs17603886
Varsomers17603886
Maprs17603886
PheGenIrs17603886
hapmaprs17603886
1000 genomesrs17603886
hgdprs17603886
ensemblrs17603886
gopubmedrs17603886
geneviewrs17603886
scholarrs17603886
googlers17603886
pharmgkbrs17603886
gwascentralrs17603886
openSNPrs17603886
23andMers17603886
23andMe allrs17603886
SNP Nexus

SNPshotrs17603886
SNPdbers17603886
MSV3drs17603886
GWAS Ctlgrs17603886
Max Magnitude
? (C;C) (C;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 7E-6
Odds Ratio NR NR