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rs281860519

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860519(C;C)
Make rs281860519(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271145
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860519
ebirs281860519
HLIrs281860519
Exacrs281860519
Varsomers281860519
Maprs281860519
PheGenIrs281860519
hapmaprs281860519
1000 genomesrs281860519
hgdprs281860519
ensemblrs281860519
gopubmedrs281860519
geneviewrs281860519
scholarrs281860519
googlers281860519
pharmgkbrs281860519
gwascentralrs281860519
openSNPrs281860519
23andMers281860519
23andMe allrs281860519
SNP Nexus

SNPshotrs281860519
SNPdbers281860519
MSV3drs281860519
GWAS Ctlgrs281860519
Max Magnitude0
ClinVar
Risk rs281860519(C;C)
Alt rs281860519(C;C)
Reference rs281860519(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238922A>G
CLNSRC
CLNACC