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rs7186852

From SNPedia

Orientationplus
Stabilizedplus
Make rs7186852(A;A)
Make rs7186852(A;G)
Make rs7186852(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position30624338
is asnp
is mentioned by
dbSNPrs7186852
ebirs7186852
HLIrs7186852
Exacrs7186852
Varsomers7186852
Maprs7186852
PheGenIrs7186852
hapmaprs7186852
1000 genomesrs7186852
hgdprs7186852
ensemblrs7186852
gopubmedrs7186852
geneviewrs7186852
scholarrs7186852
googlers7186852
pharmgkbrs7186852
gwascentralrs7186852
openSNPrs7186852
23andMers7186852
23andMe allrs7186852
SNP Nexus

SNPshotrs7186852
SNPdbers7186852
MSV3drs7186852
GWAS Ctlgrs7186852
GMAF0.3806
Max Magnitude
? (A;A) (A;G) (G;G) 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 A
P-val 3E-7
Odds Ratio 1.29 [1.17-1.42]


GET Evidence
rs7186852
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.420635
summary