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rs9523762

From SNPedia

Orientationplus
Stabilizedplus
Make rs9523762(A;A)
Make rs9523762(A;G)
Make rs9523762(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position92679633
GeneGPC5
is asnp
is mentioned by
dbSNPrs9523762
ebirs9523762
HLIrs9523762
Exacrs9523762
Varsomers9523762
Maprs9523762
PheGenIrs9523762
hapmaprs9523762
1000 genomesrs9523762
hgdprs9523762
ensemblrs9523762
gopubmedrs9523762
geneviewrs9523762
scholarrs9523762
googlers9523762
pharmgkbrs9523762
gwascentralrs9523762
openSNPrs9523762
23andMers9523762
23andMe allrs9523762
SNP Nexus

SNPshotrs9523762
SNPdbers9523762
MSV3drs9523762
GWAS Ctlgrs9523762
GMAF0.4376
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 0.000001
Odds Ratio 1.36 [NR]


OMIM126200
Desc
Variant
Relatedalso
[PMID 20182566OA-icon.png] The genetic aspects of multiple sclerosis.

[PMID 20405052OA-icon.png] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

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


GET Evidence
rs9523762
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.429688
summary