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rs1981626

From SNPedia

Orientationminus
Stabilizedminus
Make rs1981626(A;A)
Make rs1981626(A;G)
Make rs1981626(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position145148892
is asnp
is mentioned by
dbSNPrs1981626
ebirs1981626
HLIrs1981626
Exacrs1981626
Varsomers1981626
Maprs1981626
PheGenIrs1981626
hapmaprs1981626
1000 genomesrs1981626
hgdprs1981626
ensemblrs1981626
gopubmedrs1981626
geneviewrs1981626
scholarrs1981626
googlers1981626
pharmgkbrs1981626
gwascentralrs1981626
openSNPrs1981626
23andMers1981626
23andMe allrs1981626
SNP Nexus

SNPshotrs1981626
SNPdbers1981626
MSV3drs1981626
GWAS Ctlgrs1981626
Max Magnitude
? (A;A) (A;G) (G;G) 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