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rs281860530

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860530(A;A)
Make rs281860530(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271125
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860530
ebirs281860530
HLIrs281860530
Exacrs281860530
Varsomers281860530
Maprs281860530
PheGenIrs281860530
hapmaprs281860530
1000 genomesrs281860530
hgdprs281860530
ensemblrs281860530
gopubmedrs281860530
geneviewrs281860530
scholarrs281860530
googlers281860530
pharmgkbrs281860530
gwascentralrs281860530
openSNPrs281860530
23andMers281860530
23andMe allrs281860530
SNP Nexus

SNPshotrs281860530
SNPdbers281860530
MSV3drs281860530
GWAS Ctlgrs281860530
Max Magnitude0
ClinVar
Risk rs281860530(A;A)
Alt rs281860530(A;A)
Reference rs281860530(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238902C>T
CLNSRC
CLNACC