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rs17879990

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17879990(C;T)
Make rs17879990(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942750
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17879990
ebirs17879990
HLIrs17879990
Exacrs17879990
Varsomers17879990
Maprs17879990
PheGenIrs17879990
hapmaprs17879990
1000 genomesrs17879990
hgdprs17879990
ensemblrs17879990
gopubmedrs17879990
geneviewrs17879990
scholarrs17879990
googlers17879990
pharmgkbrs17879990
gwascentralrs17879990
openSNPrs17879990
23andMers17879990
23andMe allrs17879990
SNP Nexus

SNPshotrs17879990
SNPdbers17879990
MSV3drs17879990
GWAS Ctlgrs17879990
GMAF0.3981
Max Magnitude0
ClinVar
Risk rs17879990(T;T)
Alt rs17879990(T;T)
Reference rs17879990(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910527C>T
CLNSRC
CLNACC