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rs1929412

From SNPedia

Orientationminus
Stabilizedminus
Make rs1929412(G;G)
Make rs1929412(G;T)
Make rs1929412(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position11951222
is asnp
is mentioned by
dbSNPrs1929412
ebirs1929412
HLIrs1929412
Exacrs1929412
Varsomers1929412
Maprs1929412
PheGenIrs1929412
hapmaprs1929412
1000 genomesrs1929412
hgdprs1929412
ensemblrs1929412
gopubmedrs1929412
geneviewrs1929412
scholarrs1929412
googlers1929412
pharmgkbrs1929412
gwascentralrs1929412
openSNPrs1929412
23andMers1929412
23andMe allrs1929412
SNP Nexus

SNPshotrs1929412
SNPdbers1929412
MSV3drs1929412
GWAS Ctlgrs1929412
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 8E-6
Odds Ratio NR NR