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rs7665939

From SNPedia

Orientationplus
Stabilizedplus
Make rs7665939(C;C)
Make rs7665939(C;T)
Make rs7665939(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position189202164
is asnp
is mentioned by
dbSNPrs7665939
ebirs7665939
HLIrs7665939
Exacrs7665939
Varsomers7665939
Maprs7665939
PheGenIrs7665939
hapmaprs7665939
1000 genomesrs7665939
hgdprs7665939
ensemblrs7665939
gopubmedrs7665939
geneviewrs7665939
scholarrs7665939
googlers7665939
pharmgkbrs7665939
gwascentralrs7665939
openSNPrs7665939
23andMers7665939
23andMe allrs7665939
SNP Nexus

SNPshotrs7665939
SNPdbers7665939
MSV3drs7665939
GWAS Ctlgrs7665939
GMAF0.06566
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22959728OA-icon.png]
Trait Amyotrophic lateral sclerosis
Title Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
Risk Allele
P-val 9E-6
Odds Ratio 1.23 [1.11-1.39]