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rs17882753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17882753(C;T)
Make rs17882753(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944817
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17882753
ebirs17882753
HLIrs17882753
Exacrs17882753
Varsomers17882753
Maprs17882753
PheGenIrs17882753
hapmaprs17882753
1000 genomesrs17882753
hgdprs17882753
ensemblrs17882753
gopubmedrs17882753
geneviewrs17882753
scholarrs17882753
googlers17882753
pharmgkbrs17882753
gwascentralrs17882753
openSNPrs17882753
23andMers17882753
23andMe allrs17882753
SNP Nexus

SNPshotrs17882753
SNPdbers17882753
MSV3drs17882753
GWAS Ctlgrs17882753
GMAF0.2107
Max Magnitude0
ClinVar
Risk rs17882753(T;T)
Alt rs17882753(T;T)
Reference rs17882753(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912594C>T
CLNSRC
CLNACC