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rs12047808

From SNPedia

Orientationplus
Stabilizedplus
Make rs12047808(A;A)
Make rs12047808(A;G)
Make rs12047808(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position179500179
GeneAXDND1
is asnp
is mentioned by
dbSNPrs12047808
ebirs12047808
HLIrs12047808
Exacrs12047808
Varsomers12047808
Maprs12047808
PheGenIrs12047808
hapmaprs12047808
1000 genomesrs12047808
hgdprs12047808
ensemblrs12047808
gopubmedrs12047808
geneviewrs12047808
scholarrs12047808
googlers12047808
pharmgkbrs12047808
gwascentralrs12047808
openSNPrs12047808
23andMers12047808
23andMe allrs12047808
SNP Nexus

SNPshotrs12047808
SNPdbers12047808
MSV3drs12047808
GWAS Ctlgrs12047808
GMAF0.1538
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000006
Odds Ratio NR NR



GET Evidence
rs12047808
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.139344
summary