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rs10982990

From SNPedia

Orientationplus
Stabilizedplus
Make rs10982990(A;A)
Make rs10982990(A;G)
Make rs10982990(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position115896437
GeneLINC00474
is asnp
is mentioned by
dbSNPrs10982990
ebirs10982990
HLIrs10982990
Exacrs10982990
Varsomers10982990
Maprs10982990
PheGenIrs10982990
hapmaprs10982990
1000 genomesrs10982990
hgdprs10982990
ensemblrs10982990
gopubmedrs10982990
geneviewrs10982990
scholarrs10982990
googlers10982990
pharmgkbrs10982990
gwascentralrs10982990
openSNPrs10982990
23andMers10982990
23andMe allrs10982990
SNP Nexus

SNPshotrs10982990
SNPdbers10982990
MSV3drs10982990
GWAS Ctlgrs10982990
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 2E-6
Odds Ratio NR NR