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rs1605070

From SNPedia

Orientationminus
Stabilizedminus
Make rs1605070(G;G)
Make rs1605070(G;T)
Make rs1605070(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position51882999
is asnp
is mentioned by
dbSNPrs1605070
ebirs1605070
HLIrs1605070
Exacrs1605070
Varsomers1605070
Maprs1605070
PheGenIrs1605070
hapmaprs1605070
1000 genomesrs1605070
hgdprs1605070
ensemblrs1605070
gopubmedrs1605070
geneviewrs1605070
scholarrs1605070
googlers1605070
pharmgkbrs1605070
gwascentralrs1605070
openSNPrs1605070
23andMers1605070
23andMe allrs1605070
SNP Nexus

SNPshotrs1605070
SNPdbers1605070
MSV3drs1605070
GWAS Ctlgrs1605070
Max Magnitude
? (G;G) (G;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-9
Odds Ratio 3.95 [2.78601-5.589479]