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

rs281860441

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860441(G;G)
Make rs281860441(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271344
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860441
ebirs281860441
HLIrs281860441
Exacrs281860441
Varsomers281860441
Maprs281860441
PheGenIrs281860441
hapmaprs281860441
1000 genomesrs281860441
hgdprs281860441
ensemblrs281860441
gopubmedrs281860441
geneviewrs281860441
scholarrs281860441
googlers281860441
pharmgkbrs281860441
gwascentralrs281860441
openSNPrs281860441
23andMers281860441
23andMe allrs281860441
SNP Nexus

SNPshotrs281860441
SNPdbers281860441
MSV3drs281860441
GWAS Ctlgrs281860441
Max Magnitude0
ClinVar
Risk rs281860441(G;G)
Alt rs281860441(G;G)
Reference rs281860441(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239121A>C
CLNSRC
CLNACC