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rs10798269

From SNPedia

Orientationplus
Stabilizedplus
Make rs10798269(A;A)
Make rs10798269(A;G)
Make rs10798269(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position173340574
GeneIGHVII-15-1
is asnp
is mentioned by
dbSNPrs10798269
ebirs10798269
HLIrs10798269
Exacrs10798269
Varsomers10798269
Maprs10798269
PheGenIrs10798269
hapmaprs10798269
1000 genomesrs10798269
hgdprs10798269
ensemblrs10798269
gopubmedrs10798269
geneviewrs10798269
scholarrs10798269
googlers10798269
pharmgkbrs10798269
gwascentralrs10798269
openSNPrs10798269
23andMers10798269
23andMe allrs10798269
SNP Nexus

SNPshotrs10798269
SNPdbers10798269
MSV3drs10798269
GWAS Ctlgrs10798269
GMAF0.3678
Max Magnitude
? (A;A) (A;G) (G;G) 28
One of several SNPs found in a study of ~2,5720 female patients of European ancestry to be associated with systemic lupus erythematosus.[PMID 18204446OA-icon.png]
GWAS
SNP rs10798269
PubMedID [PMID 18204446OA-icon.png]
Condition Systemic lupus erythematosus in women
Gene Intergenic
Risk Allele
pValue 1.00E-007
OR 1.22
95% CI 1.14-1.32


[PMID 19714582] Rheumatoid arthritis does not share most of the newly identified systemic lupus erythematosus genetic factors



[PMID 19341491OA-icon.png] Genome-based prediction of common diseases: methodological considerations for future research.


[PMID 19442287OA-icon.png] Replication of recently identified systemic lupus erythematosus genetic associations: a case-control study.


GET Evidence
rs10798269
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.6875
summary