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rs281860457

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860457(A;A)
Make rs281860457(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271306
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860457
ebirs281860457
HLIrs281860457
Exacrs281860457
Varsomers281860457
Maprs281860457
PheGenIrs281860457
hapmaprs281860457
1000 genomesrs281860457
hgdprs281860457
ensemblrs281860457
gopubmedrs281860457
geneviewrs281860457
scholarrs281860457
googlers281860457
pharmgkbrs281860457
gwascentralrs281860457
openSNPrs281860457
23andMers281860457
23andMe allrs281860457
SNP Nexus

SNPshotrs281860457
SNPdbers281860457
MSV3drs281860457
GWAS Ctlgrs281860457
Max Magnitude0
ClinVar
Risk rs281860457(A;A)
Alt rs281860457(A;A)
Reference rs281860457(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239083G>T
CLNSRC
CLNACC