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rs2904880

From SNPedia

Orientationplus
Stabilizedplus
Make rs2904880(C;C)
Make rs2904880(C;G)
Make rs2904880(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position28933075
GeneCD19
is asnp
is mentioned by
dbSNPrs2904880
ebirs2904880
HLIrs2904880
Exacrs2904880
Varsomers2904880
Maprs2904880
PheGenIrs2904880
hapmaprs2904880
1000 genomesrs2904880
hgdprs2904880
ensemblrs2904880
gopubmedrs2904880
geneviewrs2904880
scholarrs2904880
googlers2904880
pharmgkbrs2904880
gwascentralrs2904880
openSNPrs2904880
23andMers2904880
23andMe allrs2904880
SNP Nexus

SNPshotrs2904880
SNPdbers2904880
MSV3drs2904880
GWAS Ctlgrs2904880
GMAF0.1827
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 21961844] Association study of B-cell marker gene polymorphisms in European Caucasian patients with systemic sclerosis [PMID 19001137OA-icon.png] Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis.

GET Evidence
CD19-L174V
aa_change Leu174Val
aa_change_short L174V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.768265
summary