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rs1788776

From SNPedia

Orientationplus
Stabilizedplus
Make rs1788776(A;A)
Make rs1788776(A;G)
Make rs1788776(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position23664073
GeneANKRD29
is asnp
is mentioned by
dbSNPrs1788776
ebirs1788776
HLIrs1788776
Exacrs1788776
Varsomers1788776
Maprs1788776
PheGenIrs1788776
hapmaprs1788776
1000 genomesrs1788776
hgdprs1788776
ensemblrs1788776
gopubmedrs1788776
geneviewrs1788776
scholarrs1788776
googlers1788776
pharmgkbrs1788776
gwascentralrs1788776
openSNPrs1788776
23andMers1788776
23andMe allrs1788776
SNP Nexus

SNPshotrs1788776
SNPdbers1788776
MSV3drs1788776
GWAS Ctlgrs1788776
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24256812OA-icon.png]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
Risk Allele A
P-val 8E-6
Odds Ratio 1.11 [1.06-1.16]