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rs397020

From SNPedia

Orientationminus
Stabilizedplus
Make rs397020(A;A)
Make rs397020(A;G)
Make rs397020(G;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position1225242
GeneRAD21L1
is asnp
is mentioned by
dbSNPrs397020
ebirs397020
HLIrs397020
Exacrs397020
Varsomers397020
Maprs397020
PheGenIrs397020
hapmaprs397020
1000 genomesrs397020
hgdprs397020
ensemblrs397020
gopubmedrs397020
geneviewrs397020
scholarrs397020
googlers397020
pharmgkbrs397020
gwascentralrs397020
openSNPrs397020
23andMers397020
23andMe allrs397020
SNP Nexus

SNPshotrs397020
SNPdbers397020
MSV3drs397020
GWAS Ctlgrs397020
GMAF0.4711
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 8E-7
Odds Ratio 1.41 [NR]



[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.


GET Evidence
rs397020
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.65873
summary