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rs2842483

From SNPedia

Orientationminus
Stabilizedminus
Make rs2842483(C;C)
Make rs2842483(C;T)
Make rs2842483(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position76291234
GenePCSK5
is asnp
is mentioned by
dbSNPrs2842483
ebirs2842483
HLIrs2842483
Exacrs2842483
Varsomers2842483
Maprs2842483
PheGenIrs2842483
hapmaprs2842483
1000 genomesrs2842483
hgdprs2842483
ensemblrs2842483
gopubmedrs2842483
geneviewrs2842483
scholarrs2842483
googlers2842483
pharmgkbrs2842483
gwascentralrs2842483
openSNPrs2842483
23andMers2842483
23andMe allrs2842483
SNP Nexus

SNPshotrs2842483
SNPdbers2842483
MSV3drs2842483
GWAS Ctlgrs2842483
GMAF0.2268
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (age of onset)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000005
Odds Ratio NR NR



GET Evidence
rs2842483
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.335938
summary