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rs17886880

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17886880(C;T)
Make rs17886880(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269926
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17886880
ebirs17886880
HLIrs17886880
Exacrs17886880
Varsomers17886880
Maprs17886880
PheGenIrs17886880
hapmaprs17886880
1000 genomesrs17886880
hgdprs17886880
ensemblrs17886880
gopubmedrs17886880
geneviewrs17886880
scholarrs17886880
googlers17886880
pharmgkbrs17886880
gwascentralrs17886880
openSNPrs17886880
23andMers17886880
23andMe allrs17886880
SNP Nexus

SNPshotrs17886880
SNPdbers17886880
MSV3drs17886880
GWAS Ctlgrs17886880
GMAF0.399
Max Magnitude0
ClinVar
Risk rs17886880(T;T)
Alt rs17886880(T;T)
Reference rs17886880(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237703G>A
CLNSRC
CLNACC