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

rs281860518

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860518(C;T)
Make rs281860518(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271146
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860518
ebirs281860518
HLIrs281860518
Exacrs281860518
Varsomers281860518
Maprs281860518
PheGenIrs281860518
hapmaprs281860518
1000 genomesrs281860518
hgdprs281860518
ensemblrs281860518
gopubmedrs281860518
geneviewrs281860518
scholarrs281860518
googlers281860518
pharmgkbrs281860518
gwascentralrs281860518
openSNPrs281860518
23andMers281860518
23andMe allrs281860518
SNP Nexus

SNPshotrs281860518
SNPdbers281860518
MSV3drs281860518
GWAS Ctlgrs281860518
Max Magnitude0
ClinVar
Risk rs281860518(G,T;G,T)
Alt rs281860518(G,T;G,T)
Reference rs281860518(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238923G>A; NC_000006.11:g.31238923G>C
CLNSRC
CLNACC