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rs281860502

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860502(A;G)
Make rs281860502(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271189
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860502
ebirs281860502
HLIrs281860502
Exacrs281860502
Varsomers281860502
Maprs281860502
PheGenIrs281860502
hapmaprs281860502
1000 genomesrs281860502
hgdprs281860502
ensemblrs281860502
gopubmedrs281860502
geneviewrs281860502
scholarrs281860502
googlers281860502
pharmgkbrs281860502
gwascentralrs281860502
openSNPrs281860502
23andMers281860502
23andMe allrs281860502
SNP Nexus

SNPshotrs281860502
SNPdbers281860502
MSV3drs281860502
GWAS Ctlgrs281860502
Max Magnitude0
ClinVar
Risk rs281860502(G;G)
Alt rs281860502(G;G)
Reference rs281860502(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238966T>C
CLNSRC
CLNACC