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rs281860537

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860537(A;G)
Make rs281860537(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271110
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860537
ebirs281860537
HLIrs281860537
Exacrs281860537
Varsomers281860537
Maprs281860537
PheGenIrs281860537
hapmaprs281860537
1000 genomesrs281860537
hgdprs281860537
ensemblrs281860537
gopubmedrs281860537
geneviewrs281860537
scholarrs281860537
googlers281860537
pharmgkbrs281860537
gwascentralrs281860537
openSNPrs281860537
23andMers281860537
23andMe allrs281860537
SNP Nexus

SNPshotrs281860537
SNPdbers281860537
MSV3drs281860537
GWAS Ctlgrs281860537
Max Magnitude0
ClinVar
Risk rs281860537(G;G)
Alt rs281860537(G;G)
Reference rs281860537(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238887T>C
CLNSRC
CLNACC