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rs4799088

From SNPedia

Orientationplus
Stabilizedplus
Make rs4799088(A;A)
Make rs4799088(A;G)
Make rs4799088(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position79813548
is asnp
is mentioned by
dbSNPrs4799088
ebirs4799088
HLIrs4799088
Exacrs4799088
Varsomers4799088
Maprs4799088
PheGenIrs4799088
hapmaprs4799088
1000 genomesrs4799088
hgdprs4799088
ensemblrs4799088
gopubmedrs4799088
geneviewrs4799088
scholarrs4799088
googlers4799088
pharmgkbrs4799088
gwascentralrs4799088
openSNPrs4799088
23andMers4799088
23andMe allrs4799088
SNP Nexus

SNPshotrs4799088
SNPdbers4799088
MSV3drs4799088
GWAS Ctlgrs4799088
GMAF0.376
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20801717OA-icon.png]
Trait
Title Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
Risk Allele
P-val 0.000009
Odds Ratio 1.1500 [NR]