Have questions? Visit https://www.reddit.com/r/SNPedia

rs17880655

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17880655(C;T)
Make rs17880655(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271558
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17880655
ebirs17880655
HLIrs17880655
Exacrs17880655
Varsomers17880655
Maprs17880655
PheGenIrs17880655
hapmaprs17880655
1000 genomesrs17880655
hgdprs17880655
ensemblrs17880655
gopubmedrs17880655
geneviewrs17880655
scholarrs17880655
googlers17880655
pharmgkbrs17880655
gwascentralrs17880655
openSNPrs17880655
23andMers17880655
23andMe allrs17880655
SNP Nexus

SNPshotrs17880655
SNPdbers17880655
MSV3drs17880655
GWAS Ctlgrs17880655
GMAF0.2172
Max Magnitude0
ClinVar
Risk rs17880655(T;T)
Alt rs17880655(T;T)
Reference rs17880655(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239335G>A
CLNSRC
CLNACC