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rs8049603

From SNPedia

Orientationplus
Stabilizedplus
Make rs8049603(G;G)
Make rs8049603(G;T)
Make rs8049603(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position23055939
is asnp
is mentioned by
dbSNPrs8049603
ebirs8049603
HLIrs8049603
Exacrs8049603
Varsomers8049603
Maprs8049603
PheGenIrs8049603
hapmaprs8049603
1000 genomesrs8049603
hgdprs8049603
ensemblrs8049603
gopubmedrs8049603
geneviewrs8049603
scholarrs8049603
googlers8049603
pharmgkbrs8049603
gwascentralrs8049603
openSNPrs8049603
23andMers8049603
23andMe allrs8049603
SNP Nexus

SNPshotrs8049603
SNPdbers8049603
MSV3drs8049603
GWAS Ctlgrs8049603
GMAF0.2107
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19525955]
Trait Multiple sclerosis
Title Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
Risk Allele T
P-val 0.000001
Odds Ratio 1.19 [NR]
GET Evidence
rs8049603
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.84375
summary