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rs281860482

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860482(C;T)
Make rs281860482(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271245
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860482
ebirs281860482
HLIrs281860482
Exacrs281860482
Varsomers281860482
Maprs281860482
PheGenIrs281860482
hapmaprs281860482
1000 genomesrs281860482
hgdprs281860482
ensemblrs281860482
gopubmedrs281860482
geneviewrs281860482
scholarrs281860482
googlers281860482
pharmgkbrs281860482
gwascentralrs281860482
openSNPrs281860482
23andMers281860482
23andMe allrs281860482
SNP Nexus

SNPshotrs281860482
SNPdbers281860482
MSV3drs281860482
GWAS Ctlgrs281860482
Max Magnitude0
ClinVar
Risk rs281860482(T;T)
Alt rs281860482(T;T)
Reference rs281860482(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239022G>A
CLNSRC
CLNACC