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

rs17884390

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17884390(C;T)
Make rs17884390(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270718
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17884390
ebirs17884390
HLIrs17884390
Exacrs17884390
Varsomers17884390
Maprs17884390
PheGenIrs17884390
hapmaprs17884390
1000 genomesrs17884390
hgdprs17884390
ensemblrs17884390
gopubmedrs17884390
geneviewrs17884390
scholarrs17884390
googlers17884390
pharmgkbrs17884390
gwascentralrs17884390
openSNPrs17884390
23andMers17884390
23andMe allrs17884390
SNP Nexus

SNPshotrs17884390
SNPdbers17884390
MSV3drs17884390
GWAS Ctlgrs17884390
GMAF0.05005
Max Magnitude0
ClinVar
Risk rs17884390(T;T)
Alt rs17884390(T;T)
Reference rs17884390(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238495G>A
CLNSRC
CLNACC