Have questions? Visit https://www.reddit.com/r/SNPedia

rs281860443

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860443(A;G)
Make rs281860443(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271340
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860443
ebirs281860443
HLIrs281860443
Exacrs281860443
Varsomers281860443
Maprs281860443
PheGenIrs281860443
hapmaprs281860443
1000 genomesrs281860443
hgdprs281860443
ensemblrs281860443
gopubmedrs281860443
geneviewrs281860443
scholarrs281860443
googlers281860443
pharmgkbrs281860443
gwascentralrs281860443
openSNPrs281860443
23andMers281860443
23andMe allrs281860443
SNP Nexus

SNPshotrs281860443
SNPdbers281860443
MSV3drs281860443
GWAS Ctlgrs281860443
Max Magnitude0
ClinVar
Risk rs281860443(G;G)
Alt rs281860443(G;G)
Reference rs281860443(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239117T>C
CLNSRC
CLNACC