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rs776776

From SNPedia

Orientationminus
Stabilizedminus
Make rs776776(C;C)
Make rs776776(C;T)
Make rs776776(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position18657560
GeneADAMTSL1, LOC102724102
is asnp
is mentioned by
dbSNPrs776776
ebirs776776
HLIrs776776
Exacrs776776
Varsomers776776
Maprs776776
PheGenIrs776776
hapmaprs776776
1000 genomesrs776776
hgdprs776776
ensemblrs776776
gopubmedrs776776
geneviewrs776776
scholarrs776776
googlers776776
pharmgkbrs776776
gwascentralrs776776
openSNPrs776776
23andMers776776
23andMe allrs776776
SNP Nexus

SNPshotrs776776
SNPdbers776776
MSV3drs776776
GWAS Ctlgrs776776
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 2E-6
Odds Ratio NR NR