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rs10984447

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 2 >1.17x increased risk for multiple sclerosis
(A;G) 2 1.17x increased risk for multiple sclerosis
(G;G) 1 Normal risk for multiple sclerosis
ReferenceGRCh38 38.1/141
Chromosome9
Position119222275
GeneBRINP1
is asnp
is mentioned by
dbSNPrs10984447
dbSNP (classic)rs10984447
ClinGenrs10984447
ebirs10984447
HLIrs10984447
Exacrs10984447
Gnomadrs10984447
Varsomers10984447
LitVarrs10984447
Maprs10984447
PheGenIrs10984447
Biobankrs10984447
1000 genomesrs10984447
hgdprs10984447
ensemblrs10984447
geneviewrs10984447
scholarrs10984447
googlers10984447
pharmgkbrs10984447
gwascentralrs10984447
openSNPrs10984447
23andMers10984447
SNPshotrs10984447
SNPdbers10984447
MSV3drs10984447
GWAS Ctlgrs10984447
GMAF0.1657
Max Magnitude2
? (A;A) (A;G) (G;G) 28


rs10984447 has been reported in a large study to be associated with multiple sclerosis.

The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with this allele is 1.17 (CI 1.09-1.25). [PMID 17660530]

GWAS
SNP rs10984447
PubMedID [PMID 17660530]
Condition Multiple sclerosis
Gene DBC1
Risk Allele A
pValue 8.00E-006
OR 1.17
95% CI 1.09-1.25





[PMID 22492128] Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.