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rs1529316

From SNPedia

Orientationplus
Stabilizedplus
Make rs1529316(C;C)
Make rs1529316(C;T)
Make rs1529316(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position3970616
GeneCSMD1
is asnp
is mentioned by
dbSNPrs1529316
ebirs1529316
HLIrs1529316
Exacrs1529316
Varsomers1529316
Maprs1529316
PheGenIrs1529316
hapmaprs1529316
1000 genomesrs1529316
hgdprs1529316
ensemblrs1529316
gopubmedrs1529316
geneviewrs1529316
scholarrs1529316
googlers1529316
pharmgkbrs1529316
gwascentralrs1529316
openSNPrs1529316
23andMers1529316
23andMe allrs1529316
SNP Nexus

SNPshotrs1529316
SNPdbers1529316
MSV3drs1529316
GWAS Ctlgrs1529316
GMAF0.3829
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000002
Odds Ratio 1.36 [NR]


[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.


GET Evidence
rs1529316
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.523438
summary