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rs2667100

From SNPedia

Orientationplus
Stabilizedplus
Make rs2667100(A;A)
Make rs2667100(A;G)
Make rs2667100(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position142054920
GeneINPP4B
is asnp
is mentioned by
dbSNPrs2667100
ebirs2667100
HLIrs2667100
Exacrs2667100
Varsomers2667100
Maprs2667100
PheGenIrs2667100
hapmaprs2667100
1000 genomesrs2667100
hgdprs2667100
ensemblrs2667100
gopubmedrs2667100
geneviewrs2667100
scholarrs2667100
googlers2667100
pharmgkbrs2667100
gwascentralrs2667100
openSNPrs2667100
23andMers2667100
23andMe allrs2667100
SNP Nexus

SNPshotrs2667100
SNPdbers2667100
MSV3drs2667100
GWAS Ctlgrs2667100
Max Magnitude
? (A;A) (A;G) (G;G) 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 9E-7
Odds Ratio NR NR