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rs17880291

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs17880291(G;G)
Make rs17880291(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944785
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17880291
ebirs17880291
HLIrs17880291
Exacrs17880291
Varsomers17880291
Maprs17880291
PheGenIrs17880291
hapmaprs17880291
1000 genomesrs17880291
hgdprs17880291
ensemblrs17880291
gopubmedrs17880291
geneviewrs17880291
scholarrs17880291
googlers17880291
pharmgkbrs17880291
gwascentralrs17880291
openSNPrs17880291
23andMers17880291
23andMe allrs17880291
SNP Nexus

SNPshotrs17880291
SNPdbers17880291
MSV3drs17880291
GWAS Ctlgrs17880291
GMAF0.1465
Max Magnitude0
ClinVar
Risk rs17880291(G;G)
Alt rs17880291(G;G)
Reference rs17880291(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912562T>G
CLNSRC
CLNACC