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rs281860428

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860428(C;T)
Make rs281860428(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271611
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860428
ebirs281860428
HLIrs281860428
Exacrs281860428
Varsomers281860428
Maprs281860428
PheGenIrs281860428
hapmaprs281860428
1000 genomesrs281860428
hgdprs281860428
ensemblrs281860428
gopubmedrs281860428
geneviewrs281860428
scholarrs281860428
googlers281860428
pharmgkbrs281860428
gwascentralrs281860428
openSNPrs281860428
23andMers281860428
23andMe allrs281860428
SNP Nexus

SNPshotrs281860428
SNPdbers281860428
MSV3drs281860428
GWAS Ctlgrs281860428
Max Magnitude0
ClinVar
Risk rs281860428(T;T)
Alt rs281860428(T;T)
Reference rs281860428(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239388G>A
CLNSRC
CLNACC