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rs4363506

From SNPedia

Orientationplus
Stabilizedplus
Make rs4363506(C;C)
Make rs4363506(C;T)
Make rs4363506(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position127476239
is asnp
is mentioned by
dbSNPrs4363506
ebirs4363506
HLIrs4363506
Exacrs4363506
Varsomers4363506
Maprs4363506
PheGenIrs4363506
hapmaprs4363506
1000 genomesrs4363506
hgdprs4363506
ensemblrs4363506
gopubmedrs4363506
geneviewrs4363506
scholarrs4363506
googlers4363506
pharmgkbrs4363506
gwascentralrs4363506
openSNPrs4363506
23andMers4363506
23andMe allrs4363506
SNP Nexus

SNPshotrs4363506
SNPdbers4363506
MSV3drs4363506
GWAS Ctlgrs4363506
GMAF0.4789
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs4363506
PubMedID [PMID 17362836]
Condition Amyotrophic lateral sclerosis
Gene Intergenic
Risk Allele
pValue 7.00E-007
OR 1.9
95% CI 1.50-2.40


[PMID 19740415OA-icon.png] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis



GET Evidence
rs4363506
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.460317
summary