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rs281860410

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860410(C;T)
Make rs281860410(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271648
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860410
ebirs281860410
HLIrs281860410
Exacrs281860410
Varsomers281860410
Maprs281860410
PheGenIrs281860410
hapmaprs281860410
1000 genomesrs281860410
hgdprs281860410
ensemblrs281860410
gopubmedrs281860410
geneviewrs281860410
scholarrs281860410
googlers281860410
pharmgkbrs281860410
gwascentralrs281860410
openSNPrs281860410
23andMers281860410
23andMe allrs281860410
SNP Nexus

SNPshotrs281860410
SNPdbers281860410
MSV3drs281860410
GWAS Ctlgrs281860410
Max Magnitude0
ClinVar
Risk rs281860410(T;T)
Alt rs281860410(T;T)
Reference rs281860410(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239425G>A
CLNSRC
CLNACC