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rs1147246

From SNPedia

Orientationplus
Stabilizedplus
Make rs1147246(G;G)
Make rs1147246(G;T)
Make rs1147246(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position125390920
GeneTMEM132B
is asnp
is mentioned by
dbSNPrs1147246
ebirs1147246
HLIrs1147246
Exacrs1147246
Varsomers1147246
Maprs1147246
PheGenIrs1147246
hapmaprs1147246
1000 genomesrs1147246
hgdprs1147246
ensemblrs1147246
gopubmedrs1147246
geneviewrs1147246
scholarrs1147246
googlers1147246
pharmgkbrs1147246
gwascentralrs1147246
openSNPrs1147246
23andMers1147246
23andMe allrs1147246
SNP Nexus

SNPshotrs1147246
SNPdbers1147246
MSV3drs1147246
GWAS Ctlgrs1147246
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 2E-6
Odds Ratio NR NR