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rs17881458

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17881458(C;T)
Make rs17881458(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269460
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17881458
ebirs17881458
HLIrs17881458
Exacrs17881458
Varsomers17881458
Maprs17881458
PheGenIrs17881458
hapmaprs17881458
1000 genomesrs17881458
hgdprs17881458
ensemblrs17881458
gopubmedrs17881458
geneviewrs17881458
scholarrs17881458
googlers17881458
pharmgkbrs17881458
gwascentralrs17881458
openSNPrs17881458
23andMers17881458
23andMe allrs17881458
SNP Nexus

SNPshotrs17881458
SNPdbers17881458
MSV3drs17881458
GWAS Ctlgrs17881458
GMAF0.02709
Max Magnitude0
ClinVar
Risk rs17881458(T;T)
Alt rs17881458(T;T)
Reference rs17881458(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237237G>A
CLNSRC
CLNACC