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rs3219018

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs3219018(C;C)
Make rs3219018(C;G)
ReferenceGRCh37 37.1/131
Chromosome1
Position161550842
GeneFCGR2C
is asnp
is mentioned by
dbSNPrs3219018
ebirs3219018
HLIrs3219018
Exacrs3219018
Varsomers3219018
Maprs3219018
PheGenIrs3219018
hapmaprs3219018
1000 genomesrs3219018
hgdprs3219018
ensemblrs3219018
gopubmedrs3219018
geneviewrs3219018
scholarrs3219018
googlers3219018
pharmgkbrs3219018
gwascentralrs3219018
openSNPrs3219018
23andMers3219018
23andMe allrs3219018
SNP Nexus

SNPshotrs3219018
SNPdbers3219018
MSV3drs3219018
GWAS Ctlgrs3219018
Max Magnitude0
OMIM604590
DescSYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO
Variant0001
Relatedalso
[PMID 15895258] Decreased transcription of the human FCGR2B gene mediated by the -343 G/C promoter polymorphism and association with systemic lupus erythematosus.

[PMID 18759263OA-icon.png] Features associated with, and the impact of, hemolytic anemia in patients with systemic lupus erythematosus: LX, results from a multiethnic cohort.