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rs17886232

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17886232(C;G)
Make rs17886232(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270188
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17886232
ebirs17886232
HLIrs17886232
Exacrs17886232
Varsomers17886232
Maprs17886232
PheGenIrs17886232
hapmaprs17886232
1000 genomesrs17886232
hgdprs17886232
ensemblrs17886232
gopubmedrs17886232
geneviewrs17886232
scholarrs17886232
googlers17886232
pharmgkbrs17886232
gwascentralrs17886232
openSNPrs17886232
23andMers17886232
23andMe allrs17886232
SNP Nexus

SNPshotrs17886232
SNPdbers17886232
MSV3drs17886232
GWAS Ctlgrs17886232
GMAF0.3017
Max Magnitude0
ClinVar
Risk rs17886232(G;G)
Alt rs17886232(G;G)
Reference rs17886232(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237965G>C
CLNSRC
CLNACC