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rs7672826

From SNPedia

Orientationplus
Stabilizedplus
Make rs7672826(A;A)
Make rs7672826(A;G)
Make rs7672826(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position181478542
is asnp
is mentioned by
dbSNPrs7672826
ebirs7672826
HLIrs7672826
Exacrs7672826
Varsomers7672826
Maprs7672826
PheGenIrs7672826
hapmaprs7672826
1000 genomesrs7672826
hgdprs7672826
ensemblrs7672826
gopubmedrs7672826
geneviewrs7672826
scholarrs7672826
googlers7672826
pharmgkbrs7672826
gwascentralrs7672826
openSNPrs7672826
23andMers7672826
23andMe allrs7672826
SNP Nexus

SNPshotrs7672826
SNPdbers7672826
MSV3drs7672826
GWAS Ctlgrs7672826
GMAF0.3577
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 0.000008
Odds Ratio 1.37 [NR]



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


GET Evidence
rs7672826
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.387097
summary