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rs17879496

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17879496(C;T)
Make rs17879496(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944936
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17879496
ebirs17879496
HLIrs17879496
Exacrs17879496
Varsomers17879496
Maprs17879496
PheGenIrs17879496
hapmaprs17879496
1000 genomesrs17879496
hgdprs17879496
ensemblrs17879496
gopubmedrs17879496
geneviewrs17879496
scholarrs17879496
googlers17879496
pharmgkbrs17879496
gwascentralrs17879496
openSNPrs17879496
23andMers17879496
23andMe allrs17879496
SNP Nexus

SNPshotrs17879496
SNPdbers17879496
MSV3drs17879496
GWAS Ctlgrs17879496
GMAF0.1644
Max Magnitude0
ClinVar
Risk rs17879496(T;T)
Alt rs17879496(T;T)
Reference rs17879496(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912713C>T
CLNSRC
CLNACC