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rs7191888

From SNPedia

Orientationplus
Stabilizedplus
Make rs7191888(A;A)
Make rs7191888(A;G)
Make rs7191888(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position73547159
GeneLOC101927998
is asnp
is mentioned by
dbSNPrs7191888
ebirs7191888
HLIrs7191888
Exacrs7191888
Varsomers7191888
Maprs7191888
PheGenIrs7191888
hapmaprs7191888
1000 genomesrs7191888
hgdprs7191888
ensemblrs7191888
gopubmedrs7191888
geneviewrs7191888
scholarrs7191888
googlers7191888
pharmgkbrs7191888
gwascentralrs7191888
openSNPrs7191888
23andMers7191888
23andMe allrs7191888
SNP Nexus

SNPshotrs7191888
SNPdbers7191888
MSV3drs7191888
GWAS Ctlgrs7191888
GMAF0.1878
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
rs7191888
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.273438
summary