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rs882300

From SNPedia

Orientationminus
Stabilizedminus
Make rs882300(A;A)
Make rs882300(A;G)
Make rs882300(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position136218685
is asnp
is mentioned by
dbSNPrs882300
ebirs882300
HLIrs882300
Exacrs882300
Varsomers882300
Maprs882300
PheGenIrs882300
hapmaprs882300
1000 genomesrs882300
hgdprs882300
ensemblrs882300
gopubmedrs882300
geneviewrs882300
scholarrs882300
googlers882300
pharmgkbrs882300
gwascentralrs882300
openSNPrs882300
23andMers882300
23andMe allrs882300
SNP Nexus

SNPshotrs882300
SNPdbers882300
MSV3drs882300
GWAS Ctlgrs882300
GMAF0.2755
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs882300
PubMedID [PMID 17903306OA-icon.png]
Condition Electrocardiographic traits
Gene Intergenic
Risk Allele
pValue 3.00E-007
OR NA
95% CI


GWAS snp
PMID [PMID 19525953OA-icon.png]
Trait Multiple sclerosis
Title Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
Risk Allele C
P-val 1E-7
Odds Ratio 1.19 [1.09-1.30]



GET Evidence
rs882300
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.679688
summary