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rs7755729

From SNPedia

Orientationplus
Stabilizedplus
Make rs7755729(C;C)
Make rs7755729(C;T)
Make rs7755729(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position129462497
GeneLAMA2
is asnp
is mentioned by
dbSNPrs7755729
ebirs7755729
HLIrs7755729
Exacrs7755729
Varsomers7755729
Maprs7755729
PheGenIrs7755729
hapmaprs7755729
1000 genomesrs7755729
hgdprs7755729
ensemblrs7755729
gopubmedrs7755729
geneviewrs7755729
scholarrs7755729
googlers7755729
pharmgkbrs7755729
gwascentralrs7755729
openSNPrs7755729
23andMers7755729
23andMe allrs7755729
SNP Nexus

SNPshotrs7755729
SNPdbers7755729
MSV3drs7755729
GWAS Ctlgrs7755729
Max Magnitude
? (C;C) (C;T) (T;T) 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 3E-6
Odds Ratio NR NR