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rs34592426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs34592426(C;C)
Make rs34592426(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271313
GeneHLA-C
is asnp
is mentioned by
dbSNPrs34592426
ebirs34592426
HLIrs34592426
Exacrs34592426
Varsomers34592426
Maprs34592426
PheGenIrs34592426
hapmaprs34592426
1000 genomesrs34592426
hgdprs34592426
ensemblrs34592426
gopubmedrs34592426
geneviewrs34592426
scholarrs34592426
googlers34592426
pharmgkbrs34592426
gwascentralrs34592426
openSNPrs34592426
23andMers34592426
23andMe allrs34592426
SNP Nexus

SNPshotrs34592426
SNPdbers34592426
MSV3drs34592426
GWAS Ctlgrs34592426
GMAF0.1125
Max Magnitude0
ClinVar
Risk rs34592426(A,C;A,C)
Alt rs34592426(A,C;A,C)
Reference rs34592426(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239090G>A; NC_000006.11:g.31239090G>C
CLNSRC
CLNACC