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rs180358

From SNPedia

Orientationminus
Stabilizedplus
Make rs180358(A;A)
Make rs180358(A;G)
Make rs180358(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position116728676
is asnp
is mentioned by
dbSNPrs180358
ebirs180358
HLIrs180358
Exacrs180358
Varsomers180358
Maprs180358
PheGenIrs180358
hapmaprs180358
1000 genomesrs180358
hgdprs180358
ensemblrs180358
gopubmedrs180358
geneviewrs180358
scholarrs180358
googlers180358
pharmgkbrs180358
gwascentralrs180358
openSNPrs180358
23andMers180358
23andMe allrs180358
SNP Nexus

SNPshotrs180358
SNPdbers180358
MSV3drs180358
GWAS Ctlgrs180358
GMAF0.1419
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (severity)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000006
Odds Ratio NR NR



GET Evidence
rs180358
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.140625
summary