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rs281860538

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860538(A;G)
Make rs281860538(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271108
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860538
ebirs281860538
HLIrs281860538
Exacrs281860538
Varsomers281860538
Maprs281860538
PheGenIrs281860538
hapmaprs281860538
1000 genomesrs281860538
hgdprs281860538
ensemblrs281860538
gopubmedrs281860538
geneviewrs281860538
scholarrs281860538
googlers281860538
pharmgkbrs281860538
gwascentralrs281860538
openSNPrs281860538
23andMers281860538
23andMe allrs281860538
SNP Nexus

SNPshotrs281860538
SNPdbers281860538
MSV3drs281860538
GWAS Ctlgrs281860538
Max Magnitude0
ClinVar
Risk rs281860538(G;G)
Alt rs281860538(G;G)
Reference rs281860538(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238885T>C
CLNSRC
CLNACC