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rs17884428

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17884428(A;A)
Make rs17884428(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270982
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17884428
ebirs17884428
HLIrs17884428
Exacrs17884428
Varsomers17884428
Maprs17884428
PheGenIrs17884428
hapmaprs17884428
1000 genomesrs17884428
hgdprs17884428
ensemblrs17884428
gopubmedrs17884428
geneviewrs17884428
scholarrs17884428
googlers17884428
pharmgkbrs17884428
gwascentralrs17884428
openSNPrs17884428
23andMers17884428
23andMe allrs17884428
SNP Nexus

SNPshotrs17884428
SNPdbers17884428
MSV3drs17884428
GWAS Ctlgrs17884428
GMAF0.3287
Max Magnitude0
ClinVar
Risk rs17884428(A;A)
Alt rs17884428(A;A)
Reference rs17884428(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238759C>T
CLNSRC
CLNACC