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rs7830371

From SNPedia

Orientationplus
Stabilizedplus
Make rs7830371(G;G)
Make rs7830371(G;T)
Make rs7830371(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position61143108
is asnp
is mentioned by
dbSNPrs7830371
ebirs7830371
HLIrs7830371
Exacrs7830371
Varsomers7830371
Maprs7830371
PheGenIrs7830371
hapmaprs7830371
1000 genomesrs7830371
hgdprs7830371
ensemblrs7830371
gopubmedrs7830371
geneviewrs7830371
scholarrs7830371
googlers7830371
pharmgkbrs7830371
gwascentralrs7830371
openSNPrs7830371
23andMers7830371
23andMe allrs7830371
SNP Nexus

SNPshotrs7830371
SNPdbers7830371
MSV3drs7830371
GWAS Ctlgrs7830371
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 8E-7
Odds Ratio NR NR