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rs9271100

From SNPedia

Orientationplus
Stabilizedplus
Make rs9271100(C;C)
Make rs9271100(C;T)
Make rs9271100(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32608701
is asnp
is mentioned by
dbSNPrs9271100
ebirs9271100
HLIrs9271100
Exacrs9271100
Varsomers9271100
Maprs9271100
PheGenIrs9271100
hapmaprs9271100
1000 genomesrs9271100
hgdprs9271100
ensemblrs9271100
gopubmedrs9271100
geneviewrs9271100
scholarrs9271100
googlers9271100
pharmgkbrs9271100
gwascentralrs9271100
openSNPrs9271100
23andMers9271100
23andMe allrs9271100
SNP Nexus

SNPshotrs9271100
SNPdbers9271100
MSV3drs9271100
GWAS Ctlgrs9271100
GMAF0.2498
Max Magnitude


[PMID 25642632] Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy.

? (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
P-val 1E-12
Odds Ratio 1.90 [1.59-2.27]


GET Evidence
rs9271100
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.596154
summary