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rs281860548

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860548(C;T)
Make rs281860548(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271077
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860548
ebirs281860548
HLIrs281860548
Exacrs281860548
Varsomers281860548
Maprs281860548
PheGenIrs281860548
hapmaprs281860548
1000 genomesrs281860548
hgdprs281860548
ensemblrs281860548
gopubmedrs281860548
geneviewrs281860548
scholarrs281860548
googlers281860548
pharmgkbrs281860548
gwascentralrs281860548
openSNPrs281860548
23andMers281860548
23andMe allrs281860548
SNP Nexus

SNPshotrs281860548
SNPdbers281860548
MSV3drs281860548
GWAS Ctlgrs281860548
Max Magnitude0
ClinVar
Risk rs281860548(T;T)
Alt rs281860548(T;T)
Reference rs281860548(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238854G>A
CLNSRC
CLNACC