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rs1335532

From SNPedia

Orientationminus
Stabilizedminus
Make rs1335532(C;C)
Make rs1335532(C;T)
Make rs1335532(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position116558335
GeneCD58
is asnp
is mentioned by
dbSNPrs1335532
ebirs1335532
HLIrs1335532
Exacrs1335532
Varsomers1335532
Maprs1335532
PheGenIrs1335532
hapmaprs1335532
1000 genomesrs1335532
hgdprs1335532
ensemblrs1335532
gopubmedrs1335532
geneviewrs1335532
scholarrs1335532
googlers1335532
pharmgkbrs1335532
gwascentralrs1335532
openSNPrs1335532
23andMers1335532
23andMe allrs1335532
SNP Nexus

SNPshotrs1335532
SNPdbers1335532
MSV3drs1335532
GWAS Ctlgrs1335532
GMAF0.382
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19525955]
Trait Multiple sclerosis
Title Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
Risk Allele A
P-val 1E-7
Odds Ratio 1.28 [NR]


[PMID 20405052OA-icon.png] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.


GET Evidence
rs1335532
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.375
summary



GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait Multiple sclerosis
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele A
P-val 3E-16
Odds Ratio 1.22 [1.19-1.24]


[PMID 24655566OA-icon.png] CD58 polymorphisms associated with the risk of neuromyelitis optica in a Korean population