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

rs3782455

From SNPedia

Orientationplus
Stabilizedplus
Make rs3782455(G;G)
Make rs3782455(G;T)
Make rs3782455(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position113921460
GeneRBM19
is asnp
is mentioned by
dbSNPrs3782455
ebirs3782455
HLIrs3782455
Exacrs3782455
Varsomers3782455
Maprs3782455
PheGenIrs3782455
hapmaprs3782455
1000 genomesrs3782455
hgdprs3782455
ensemblrs3782455
gopubmedrs3782455
geneviewrs3782455
scholarrs3782455
googlers3782455
pharmgkbrs3782455
gwascentralrs3782455
openSNPrs3782455
23andMers3782455
23andMe allrs3782455
SNP Nexus

SNPshotrs3782455
SNPdbers3782455
MSV3drs3782455
GWAS Ctlgrs3782455
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 6E-6
Odds Ratio NR NR