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rs17684824

From SNPedia

Orientationplus
Stabilizedplus
Make rs17684824(A;A)
Make rs17684824(A;C)
Make rs17684824(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position3546358
is asnp
is mentioned by
dbSNPrs17684824
ebirs17684824
HLIrs17684824
Exacrs17684824
Varsomers17684824
Maprs17684824
PheGenIrs17684824
hapmaprs17684824
1000 genomesrs17684824
hgdprs17684824
ensemblrs17684824
gopubmedrs17684824
geneviewrs17684824
scholarrs17684824
googlers17684824
pharmgkbrs17684824
gwascentralrs17684824
openSNPrs17684824
23andMers17684824
23andMe allrs17684824
SNP Nexus

SNPshotrs17684824
SNPdbers17684824
MSV3drs17684824
GWAS Ctlgrs17684824
Max Magnitude
? (A;A) (A;C) (C;C) 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 4E-6
Odds Ratio NR NR