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rs17884362

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17884362(A;A)
Make rs17884362(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270140
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17884362
ebirs17884362
HLIrs17884362
Exacrs17884362
Varsomers17884362
Maprs17884362
PheGenIrs17884362
hapmaprs17884362
1000 genomesrs17884362
hgdprs17884362
ensemblrs17884362
gopubmedrs17884362
geneviewrs17884362
scholarrs17884362
googlers17884362
pharmgkbrs17884362
gwascentralrs17884362
openSNPrs17884362
23andMers17884362
23andMe allrs17884362
SNP Nexus

SNPshotrs17884362
SNPdbers17884362
MSV3drs17884362
GWAS Ctlgrs17884362
GMAF0.1442
Max Magnitude0
ClinVar
Risk rs17884362(A;A)
Alt rs17884362(A;A)
Reference rs17884362(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237917C>T
CLNSRC
CLNACC