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

rs7267421

From SNPedia

Orientationplus
Stabilizedplus
Make rs7267421(A;A)
Make rs7267421(A;G)
Make rs7267421(G;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position15246990
GeneMACROD2
is asnp
is mentioned by
dbSNPrs7267421
ebirs7267421
HLIrs7267421
Exacrs7267421
Varsomers7267421
Maprs7267421
PheGenIrs7267421
hapmaprs7267421
1000 genomesrs7267421
hgdprs7267421
ensemblrs7267421
gopubmedrs7267421
geneviewrs7267421
scholarrs7267421
googlers7267421
pharmgkbrs7267421
gwascentralrs7267421
openSNPrs7267421
23andMers7267421
23andMe allrs7267421
SNP Nexus

SNPshotrs7267421
SNPdbers7267421
MSV3drs7267421
GWAS Ctlgrs7267421
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