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rs17157903

From SNPedia

Orientationplus
Stabilizedplus
Make rs17157903(C;C)
Make rs17157903(C;T)
Make rs17157903(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position103987589
GeneRELN
is asnp
is mentioned by
dbSNPrs17157903
ebirs17157903
HLIrs17157903
Exacrs17157903
Varsomers17157903
Maprs17157903
PheGenIrs17157903
hapmaprs17157903
1000 genomesrs17157903
hgdprs17157903
ensemblrs17157903
gopubmedrs17157903
geneviewrs17157903
scholarrs17157903
googlers17157903
pharmgkbrs17157903
gwascentralrs17157903
openSNPrs17157903
23andMers17157903
23andMe allrs17157903
SNP Nexus

SNPshotrs17157903
SNPdbers17157903
MSV3drs17157903
GWAS Ctlgrs17157903
GMAF0.1612
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 0.000003
Odds Ratio NR NR



[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.


GET Evidence
rs17157903
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary



[PMID 23563089OA-icon.png] Genetic ancestry modifies the association between genetic risk variants and breast cancer risk among Hispanic and non-Hispanic white women.