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rs17885779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17885779(C;T)
Make rs17885779(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944879
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17885779
ebirs17885779
HLIrs17885779
Exacrs17885779
Varsomers17885779
Maprs17885779
PheGenIrs17885779
hapmaprs17885779
1000 genomesrs17885779
hgdprs17885779
ensemblrs17885779
gopubmedrs17885779
geneviewrs17885779
scholarrs17885779
googlers17885779
pharmgkbrs17885779
gwascentralrs17885779
openSNPrs17885779
23andMers17885779
23andMe allrs17885779
SNP Nexus

SNPshotrs17885779
SNPdbers17885779
MSV3drs17885779
GWAS Ctlgrs17885779
Max Magnitude0
ClinVar
Risk rs17885779(T;T)
Alt rs17885779(T;T)
Reference rs17885779(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912656C>T
CLNSRC
CLNACC