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rs17885557

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17885557(G;T)
Make rs17885557(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269310
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17885557
ebirs17885557
HLIrs17885557
Exacrs17885557
Varsomers17885557
Maprs17885557
PheGenIrs17885557
hapmaprs17885557
1000 genomesrs17885557
hgdprs17885557
ensemblrs17885557
gopubmedrs17885557
geneviewrs17885557
scholarrs17885557
googlers17885557
pharmgkbrs17885557
gwascentralrs17885557
openSNPrs17885557
23andMers17885557
23andMe allrs17885557
SNP Nexus

SNPshotrs17885557
SNPdbers17885557
MSV3drs17885557
GWAS Ctlgrs17885557
GMAF0.1235
Max Magnitude0
ClinVar
Risk rs17885557(T;T)
Alt rs17885557(T;T)
Reference rs17885557(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237087C>A
CLNSRC
CLNACC