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rs281860588

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860588(A;A)
Make rs281860588(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269494
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860588
ClinGenrs281860588
ebirs281860588
HLIrs281860588
Exacrs281860588
Varsomers281860588
Maprs281860588
PheGenIrs281860588
hapmaprs281860588
1000 genomesrs281860588
hgdprs281860588
ensemblrs281860588
gopubmedrs281860588
geneviewrs281860588
scholarrs281860588
googlers281860588
pharmgkbrs281860588
gwascentralrs281860588
openSNPrs281860588
23andMers281860588
23andMe allrs281860588
SNP Nexus

SNPshotrs281860588
SNPdbers281860588
MSV3drs281860588
GWAS Ctlgrs281860588
Max Magnitude0
ClinVar
Risk rs281860588(A;A)
Alt rs281860588(A;A)
Reference Rs281860588(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237271C>T
CLNSRC
CLNACC