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rs281860463

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860463(C;G)
Make rs281860463(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271290
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860463
ebirs281860463
HLIrs281860463
Exacrs281860463
Varsomers281860463
Maprs281860463
PheGenIrs281860463
hapmaprs281860463
1000 genomesrs281860463
hgdprs281860463
ensemblrs281860463
gopubmedrs281860463
geneviewrs281860463
scholarrs281860463
googlers281860463
pharmgkbrs281860463
gwascentralrs281860463
openSNPrs281860463
23andMers281860463
23andMe allrs281860463
SNP Nexus

SNPshotrs281860463
SNPdbers281860463
MSV3drs281860463
GWAS Ctlgrs281860463
Max Magnitude0
ClinVar
Risk rs281860463(G;G)
Alt rs281860463(G;G)
Reference rs281860463(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239067G>C
CLNSRC
CLNACC