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rs7899101

From SNPedia

Orientationplus
Stabilizedplus
Make rs7899101(C;C)
Make rs7899101(C;T)
Make rs7899101(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position5566239
is asnp
is mentioned by
dbSNPrs7899101
ebirs7899101
HLIrs7899101
Exacrs7899101
Varsomers7899101
Maprs7899101
PheGenIrs7899101
hapmaprs7899101
1000 genomesrs7899101
hgdprs7899101
ensemblrs7899101
gopubmedrs7899101
geneviewrs7899101
scholarrs7899101
googlers7899101
pharmgkbrs7899101
gwascentralrs7899101
openSNPrs7899101
23andMers7899101
23andMe allrs7899101
SNP Nexus

SNPshotrs7899101
SNPdbers7899101
MSV3drs7899101
GWAS Ctlgrs7899101
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 3E-6
Odds Ratio NR NR