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

rs281860402

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860402(A;G)
Make rs281860402(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271667
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860402
ebirs281860402
HLIrs281860402
Exacrs281860402
Varsomers281860402
Maprs281860402
PheGenIrs281860402
hapmaprs281860402
1000 genomesrs281860402
hgdprs281860402
ensemblrs281860402
gopubmedrs281860402
geneviewrs281860402
scholarrs281860402
googlers281860402
pharmgkbrs281860402
gwascentralrs281860402
openSNPrs281860402
23andMers281860402
23andMe allrs281860402
SNP Nexus

SNPshotrs281860402
SNPdbers281860402
MSV3drs281860402
GWAS Ctlgrs281860402
Max Magnitude0
ClinVar
Risk rs281860402(G;G)
Alt rs281860402(G;G)
Reference rs281860402(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239444T>C
CLNSRC
CLNACC