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rs1386330

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1386330(C;C)
Make rs1386330(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position88086259
is asnp
is mentioned by
dbSNPrs1386330
ebirs1386330
HLIrs1386330
Exacrs1386330
Varsomers1386330
Maprs1386330
PheGenIrs1386330
hapmaprs1386330
1000 genomesrs1386330
hgdprs1386330
ensemblrs1386330
gopubmedrs1386330
geneviewrs1386330
scholarrs1386330
googlers1386330
pharmgkbrs1386330
gwascentralrs1386330
openSNPrs1386330
23andMers1386330
23andMe allrs1386330
SNP Nexus

SNPshotrs1386330
SNPdbers1386330
MSV3drs1386330
GWAS Ctlgrs1386330
GMAF0.1148
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (age of onset)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000002
Odds Ratio NR NR



GET Evidence
rs1386330
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.101562
summary