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rs281860566

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860566(A;A)
Make rs281860566(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270339
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860566
ebirs281860566
HLIrs281860566
Exacrs281860566
Varsomers281860566
Maprs281860566
PheGenIrs281860566
hapmaprs281860566
1000 genomesrs281860566
hgdprs281860566
ensemblrs281860566
gopubmedrs281860566
geneviewrs281860566
scholarrs281860566
googlers281860566
pharmgkbrs281860566
gwascentralrs281860566
openSNPrs281860566
23andMers281860566
23andMe allrs281860566
SNP Nexus

SNPshotrs281860566
SNPdbers281860566
MSV3drs281860566
GWAS Ctlgrs281860566
Max Magnitude0
ClinVar
Risk rs281860566(A;A)
Alt rs281860566(A;A)
Reference rs281860566(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238116C>T
CLNSRC
CLNACC