Have questions? Visit https://www.reddit.com/r/SNPedia

rs2972219

From SNPedia

Orientationplus
Stabilizedplus
Make rs2972219(A;A)
Make rs2972219(A;C)
Make rs2972219(C;C)
ReferenceGRCh38 38.1/142
Chromosome5
Position118647917
is asnp
is mentioned by
dbSNPrs2972219
ebirs2972219
HLIrs2972219
Exacrs2972219
Varsomers2972219
Maprs2972219
PheGenIrs2972219
hapmaprs2972219
1000 genomesrs2972219
hgdprs2972219
ensemblrs2972219
gopubmedrs2972219
geneviewrs2972219
scholarrs2972219
googlers2972219
pharmgkbrs2972219
gwascentralrs2972219
openSNPrs2972219
23andMers2972219
23andMe allrs2972219
SNP Nexus

SNPshotrs2972219
SNPdbers2972219
MSV3drs2972219
GWAS Ctlgrs2972219
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