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rs10259085

From SNPedia

Orientationplus
Stabilizedplus
Make rs10259085(C;C)
Make rs10259085(C;T)
Make rs10259085(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position7228800
GeneC1GALT1
is asnp
is mentioned by
dbSNPrs10259085
ebirs10259085
HLIrs10259085
Exacrs10259085
Varsomers10259085
Maprs10259085
PheGenIrs10259085
hapmaprs10259085
1000 genomesrs10259085
hgdprs10259085
ensemblrs10259085
gopubmedrs10259085
geneviewrs10259085
scholarrs10259085
googlers10259085
pharmgkbrs10259085
gwascentralrs10259085
openSNPrs10259085
23andMers10259085
23andMe allrs10259085
SNP Nexus

SNPshotrs10259085
SNPdbers10259085
MSV3drs10259085
GWAS Ctlgrs10259085
GMAF0.4017
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 0.000004
Odds Ratio NR NR



GET Evidence
rs10259085
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.664062
summary