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rs281860486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860486(A;A)
Make rs281860486(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271236
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860486
ebirs281860486
HLIrs281860486
Exacrs281860486
Varsomers281860486
Maprs281860486
PheGenIrs281860486
hapmaprs281860486
1000 genomesrs281860486
hgdprs281860486
ensemblrs281860486
gopubmedrs281860486
geneviewrs281860486
scholarrs281860486
googlers281860486
pharmgkbrs281860486
gwascentralrs281860486
openSNPrs281860486
23andMers281860486
23andMe allrs281860486
SNP Nexus

SNPshotrs281860486
SNPdbers281860486
MSV3drs281860486
GWAS Ctlgrs281860486
Max Magnitude0
ClinVar
Risk rs281860486(A;A)
Alt rs281860486(A;A)
Reference rs281860486(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239013C>T
CLNSRC
CLNACC