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rs34517613

From SNPedia

Orientationplus
Stabilizedplus
Make rs34517613(C;C)
Make rs34517613(C;T)
Make rs34517613(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position28283226
GeneKRT18P55
is asnp
is mentioned by
dbSNPrs34517613
ebirs34517613
HLIrs34517613
Exacrs34517613
Varsomers34517613
Maprs34517613
PheGenIrs34517613
hapmaprs34517613
1000 genomesrs34517613
hgdprs34517613
ensemblrs34517613
gopubmedrs34517613
geneviewrs34517613
scholarrs34517613
googlers34517613
pharmgkbrs34517613
gwascentralrs34517613
openSNPrs34517613
23andMers34517613
23andMe allrs34517613
SNP Nexus

SNPshotrs34517613
SNPdbers34517613
MSV3drs34517613
GWAS Ctlgrs34517613
Max Magnitude
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 T
P-val 9E-9
Odds Ratio 1.20 [1.12-1.29]