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rs7148498

From SNPedia

Orientationplus
Stabilizedplus
Make rs7148498(C;C)
Make rs7148498(C;T)
Make rs7148498(T;T)
ReferenceGRCh38 38.1/142
Chromosome14
Position95641618
is asnp
is mentioned by
dbSNPrs7148498
ebirs7148498
HLIrs7148498
Exacrs7148498
Varsomers7148498
Maprs7148498
PheGenIrs7148498
hapmaprs7148498
1000 genomesrs7148498
hgdprs7148498
ensemblrs7148498
gopubmedrs7148498
geneviewrs7148498
scholarrs7148498
googlers7148498
pharmgkbrs7148498
gwascentralrs7148498
openSNPrs7148498
23andMers7148498
23andMe allrs7148498
SNP Nexus

SNPshotrs7148498
SNPdbers7148498
MSV3drs7148498
GWAS Ctlgrs7148498
Max Magnitude
? (C;C) (C;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 1E-6
Odds Ratio NR NR