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rs2904759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2904759(C;G)
Make rs2904759(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942719
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2904759
ebirs2904759
HLIrs2904759
Exacrs2904759
Varsomers2904759
Maprs2904759
PheGenIrs2904759
hapmaprs2904759
1000 genomesrs2904759
hgdprs2904759
ensemblrs2904759
gopubmedrs2904759
geneviewrs2904759
scholarrs2904759
googlers2904759
pharmgkbrs2904759
gwascentralrs2904759
openSNPrs2904759
23andMers2904759
23andMe allrs2904759
SNP Nexus

SNPshotrs2904759
SNPdbers2904759
MSV3drs2904759
GWAS Ctlgrs2904759
GMAF0.1134
Max Magnitude0
ClinVar
Risk rs2904759(G;G)
Alt rs2904759(G;G)
Reference rs2904759(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910496C; NC_000006.11:g.29910496C>G
CLNSRC
CLNACC