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rs17885126

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs17885126(A;C)
Make rs17885126(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944787
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17885126
ebirs17885126
HLIrs17885126
Exacrs17885126
Varsomers17885126
Maprs17885126
PheGenIrs17885126
hapmaprs17885126
1000 genomesrs17885126
hgdprs17885126
ensemblrs17885126
gopubmedrs17885126
geneviewrs17885126
scholarrs17885126
googlers17885126
pharmgkbrs17885126
gwascentralrs17885126
openSNPrs17885126
23andMers17885126
23andMe allrs17885126
SNP Nexus

SNPshotrs17885126
SNPdbers17885126
MSV3drs17885126
GWAS Ctlgrs17885126
GMAF0.146
Max Magnitude0
ClinVar
Risk rs17885126(C;C)
Alt rs17885126(C;C)
Reference rs17885126(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912564A>C
CLNSRC
CLNACC