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rs7253363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs7253363(G;T)
Make rs7253363(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position11571680
GeneLOC101928434
is asnp
is mentioned by
dbSNPrs7253363
ebirs7253363
HLIrs7253363
Exacrs7253363
Varsomers7253363
Maprs7253363
PheGenIrs7253363
hapmaprs7253363
1000 genomesrs7253363
hgdprs7253363
ensemblrs7253363
gopubmedrs7253363
geneviewrs7253363
scholarrs7253363
googlers7253363
pharmgkbrs7253363
gwascentralrs7253363
openSNPrs7253363
23andMers7253363
23andMe allrs7253363
SNP Nexus

SNPshotrs7253363
SNPdbers7253363
MSV3drs7253363
GWAS Ctlgrs7253363
GMAF0.01837
Max Magnitude0
? (G;G) (G;T) (T;T) 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 0.000009
Odds Ratio NR NR



GET Evidence
rs7253363
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.984375
summary