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rs17884702

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17884702(C;T)
Make rs17884702(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270759
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17884702
ebirs17884702
HLIrs17884702
Exacrs17884702
Varsomers17884702
Maprs17884702
PheGenIrs17884702
hapmaprs17884702
1000 genomesrs17884702
hgdprs17884702
ensemblrs17884702
gopubmedrs17884702
geneviewrs17884702
scholarrs17884702
googlers17884702
pharmgkbrs17884702
gwascentralrs17884702
openSNPrs17884702
23andMers17884702
23andMe allrs17884702
SNP Nexus

SNPshotrs17884702
SNPdbers17884702
MSV3drs17884702
GWAS Ctlgrs17884702
GMAF0.05005
Max Magnitude0
ClinVar
Risk rs17884702(T;T)
Alt rs17884702(T;T)
Reference rs17884702(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238536G>A
CLNSRC
CLNACC