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rs1488902

From SNPedia

Orientationplus
Stabilizedplus
Make rs1488902(C;C)
Make rs1488902(C;T)
Make rs1488902(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position89611857
is asnp
is mentioned by
dbSNPrs1488902
ebirs1488902
HLIrs1488902
Exacrs1488902
Varsomers1488902
Maprs1488902
PheGenIrs1488902
hapmaprs1488902
1000 genomesrs1488902
hgdprs1488902
ensemblrs1488902
gopubmedrs1488902
geneviewrs1488902
scholarrs1488902
googlers1488902
pharmgkbrs1488902
gwascentralrs1488902
openSNPrs1488902
23andMers1488902
23andMe allrs1488902
SNP Nexus

SNPshotrs1488902
SNPdbers1488902
MSV3drs1488902
GWAS Ctlgrs1488902
GMAF0.3999
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20801717OA-icon.png]
Trait
Title Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
Risk Allele C
P-val 0.000003
Odds Ratio 1.1450 [NR]