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rs11666377

From SNPedia

Orientationplus
Stabilizedplus
Make rs11666377(C;C)
Make rs11666377(C;T)
Make rs11666377(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position17007623
GeneCPAMD8
is asnp
is mentioned by
dbSNPrs11666377
ebirs11666377
HLIrs11666377
Exacrs11666377
Varsomers11666377
Maprs11666377
PheGenIrs11666377
hapmaprs11666377
1000 genomesrs11666377
hgdprs11666377
ensemblrs11666377
gopubmedrs11666377
geneviewrs11666377
scholarrs11666377
googlers11666377
pharmgkbrs11666377
gwascentralrs11666377
openSNPrs11666377
23andMers11666377
23andMe allrs11666377
SNP Nexus

SNPshotrs11666377
SNPdbers11666377
MSV3drs11666377
GWAS Ctlgrs11666377
GMAF0.1552
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Brain lesion load
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000007
Odds Ratio NR NR



GET Evidence
rs11666377
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary