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rs17885436

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17885436(C;G)
Make rs17885436(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269225
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17885436
ebirs17885436
HLIrs17885436
Exacrs17885436
Varsomers17885436
Maprs17885436
PheGenIrs17885436
hapmaprs17885436
1000 genomesrs17885436
hgdprs17885436
ensemblrs17885436
gopubmedrs17885436
geneviewrs17885436
scholarrs17885436
googlers17885436
pharmgkbrs17885436
gwascentralrs17885436
openSNPrs17885436
23andMers17885436
23andMe allrs17885436
SNP Nexus

SNPshotrs17885436
SNPdbers17885436
MSV3drs17885436
GWAS Ctlgrs17885436
GMAF0.1543
Max Magnitude0
ClinVar
Risk rs17885436(G;G)
Alt rs17885436(G;G)
Reference rs17885436(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237002G>C
CLNSRC
CLNACC