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rs1927457

From SNPedia

Orientationplus
Stabilizedplus
Make rs1927457(C;C)
Make rs1927457(C;T)
Make rs1927457(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position29719734
GeneSVIL
is asnp
is mentioned by
dbSNPrs1927457
ebirs1927457
HLIrs1927457
Exacrs1927457
Varsomers1927457
Maprs1927457
PheGenIrs1927457
hapmaprs1927457
1000 genomesrs1927457
hgdprs1927457
ensemblrs1927457
gopubmedrs1927457
geneviewrs1927457
scholarrs1927457
googlers1927457
pharmgkbrs1927457
gwascentralrs1927457
openSNPrs1927457
23andMers1927457
23andMe allrs1927457
SNP Nexus

SNPshotrs1927457
SNPdbers1927457
MSV3drs1927457
GWAS Ctlgrs1927457
GMAF0.3852
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Normalized brain volume
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000008
Odds Ratio NR NR



GET Evidence
rs1927457
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary