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rs17878838

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17878838(A;A)
Make rs17878838(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943567
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17878838
ebirs17878838
HLIrs17878838
Exacrs17878838
Varsomers17878838
Maprs17878838
PheGenIrs17878838
hapmaprs17878838
1000 genomesrs17878838
hgdprs17878838
ensemblrs17878838
gopubmedrs17878838
geneviewrs17878838
scholarrs17878838
googlers17878838
pharmgkbrs17878838
gwascentralrs17878838
openSNPrs17878838
23andMers17878838
23andMe allrs17878838
SNP Nexus

SNPshotrs17878838
SNPdbers17878838
MSV3drs17878838
GWAS Ctlgrs17878838
GMAF0.1524
Max Magnitude0
ClinVar
Risk rs17878838(A,T;A,T)
Alt rs17878838(A,T;A,T)
Reference rs17878838(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911344C>A; NC_000006.11:g.29911344C>T
CLNSRC
CLNACC