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rs281860433

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860433(A;A)
Make rs281860433(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271605
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860433
ebirs281860433
HLIrs281860433
Exacrs281860433
Varsomers281860433
Maprs281860433
PheGenIrs281860433
hapmaprs281860433
1000 genomesrs281860433
hgdprs281860433
ensemblrs281860433
gopubmedrs281860433
geneviewrs281860433
scholarrs281860433
googlers281860433
pharmgkbrs281860433
gwascentralrs281860433
openSNPrs281860433
23andMers281860433
23andMe allrs281860433
SNP Nexus

SNPshotrs281860433
SNPdbers281860433
MSV3drs281860433
GWAS Ctlgrs281860433
Max Magnitude0
ClinVar
Risk rs281860433(A;A)
Alt rs281860433(A;A)
Reference rs281860433(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239382C>T
CLNSRC
CLNACC