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rs281860546

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860546(C;G)
Make rs281860546(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271085
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860546
ebirs281860546
HLIrs281860546
Exacrs281860546
Varsomers281860546
Maprs281860546
PheGenIrs281860546
hapmaprs281860546
1000 genomesrs281860546
hgdprs281860546
ensemblrs281860546
gopubmedrs281860546
geneviewrs281860546
scholarrs281860546
googlers281860546
pharmgkbrs281860546
gwascentralrs281860546
openSNPrs281860546
23andMers281860546
23andMe allrs281860546
SNP Nexus

SNPshotrs281860546
SNPdbers281860546
MSV3drs281860546
GWAS Ctlgrs281860546
Max Magnitude0
ClinVar
Risk rs281860546(G;G)
Alt rs281860546(G;G)
Reference rs281860546(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238862G>C
CLNSRC
CLNACC