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rs7812879

From SNPedia

Orientationplus
Stabilizedplus
Make rs7812879(C;C)
Make rs7812879(C;T)
Make rs7812879(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position11482672
is asnp
is mentioned by
dbSNPrs7812879
ebirs7812879
HLIrs7812879
Exacrs7812879
Varsomers7812879
Maprs7812879
PheGenIrs7812879
hapmaprs7812879
1000 genomesrs7812879
hgdprs7812879
ensemblrs7812879
gopubmedrs7812879
geneviewrs7812879
scholarrs7812879
googlers7812879
pharmgkbrs7812879
gwascentralrs7812879
openSNPrs7812879
23andMers7812879
23andMe allrs7812879
SNP Nexus

SNPshotrs7812879
SNPdbers7812879
MSV3drs7812879
GWAS Ctlgrs7812879
GMAF0.1818
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19838193]
Trait Systemic lupus erythematosus
Title Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Risk Allele G
P-val 2E-24
Odds Ratio 1.45 [1.35-1.56]
OMIM612254
Desc
Variant
Relatedalso


GET Evidence
rs7812879
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.789062
summary