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rs7224488

From SNPedia

Orientationplus
Stabilizedplus
Make rs7224488(A;A)
Make rs7224488(A;C)
Make rs7224488(C;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position56791264
is asnp
is mentioned by
dbSNPrs7224488
ebirs7224488
HLIrs7224488
Exacrs7224488
Varsomers7224488
Maprs7224488
PheGenIrs7224488
hapmaprs7224488
1000 genomesrs7224488
hgdprs7224488
ensemblrs7224488
gopubmedrs7224488
geneviewrs7224488
scholarrs7224488
googlers7224488
pharmgkbrs7224488
gwascentralrs7224488
openSNPrs7224488
23andMers7224488
23andMe allrs7224488
SNP Nexus

SNPshotrs7224488
SNPdbers7224488
MSV3drs7224488
GWAS Ctlgrs7224488
Max Magnitude
? (A;A) (A;C) (C;C) 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