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rs28749156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28749156(C;C)
Make rs28749156(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945358
GeneHLA-A
is asnp
is mentioned by
dbSNPrs28749156
ebirs28749156
HLIrs28749156
Exacrs28749156
Varsomers28749156
Maprs28749156
PheGenIrs28749156
hapmaprs28749156
1000 genomesrs28749156
hgdprs28749156
ensemblrs28749156
gopubmedrs28749156
geneviewrs28749156
scholarrs28749156
googlers28749156
pharmgkbrs28749156
gwascentralrs28749156
openSNPrs28749156
23andMers28749156
23andMe allrs28749156
SNP Nexus

SNPshotrs28749156
SNPdbers28749156
MSV3drs28749156
GWAS Ctlgrs28749156
GMAF0.315
Max Magnitude0
ClinVar
Risk rs28749156(C;C)
Alt rs28749156(C;C)
Reference rs28749156(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29913135G>C
CLNSRC
CLNACC