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rs12638253

From SNPedia

Orientationplus
Stabilizedplus
Make rs12638253(C;C)
Make rs12638253(C;T)
Make rs12638253(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position156908302
GeneLEKR1
is asnp
is mentioned by
dbSNPrs12638253
ebirs12638253
HLIrs12638253
Exacrs12638253
Varsomers12638253
Maprs12638253
PheGenIrs12638253
hapmaprs12638253
1000 genomesrs12638253
hgdprs12638253
ensemblrs12638253
gopubmedrs12638253
geneviewrs12638253
scholarrs12638253
googlers12638253
pharmgkbrs12638253
gwascentralrs12638253
openSNPrs12638253
23andMers12638253
23andMe allrs12638253
SNP Nexus

SNPshotrs12638253
SNPdbers12638253
MSV3drs12638253
GWAS Ctlgrs12638253
GMAF0.4963
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000002
Odds Ratio NR NR



[PMID 18985386OA-icon.png] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.


[PMID 19327735OA-icon.png] Genome-wide linkage screen in familial Parkinson disease identifies loci on chromosomes 3 and 18.


GET Evidence
rs12638253
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.492063
summary