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rs281860485

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860485(A;T)
Make rs281860485(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271237
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860485
ebirs281860485
HLIrs281860485
Exacrs281860485
Varsomers281860485
Maprs281860485
PheGenIrs281860485
hapmaprs281860485
1000 genomesrs281860485
hgdprs281860485
ensemblrs281860485
gopubmedrs281860485
geneviewrs281860485
scholarrs281860485
googlers281860485
pharmgkbrs281860485
gwascentralrs281860485
openSNPrs281860485
23andMers281860485
23andMe allrs281860485
SNP Nexus

SNPshotrs281860485
SNPdbers281860485
MSV3drs281860485
GWAS Ctlgrs281860485
Max Magnitude0
ClinVar
Risk rs281860485(T;T)
Alt rs281860485(T;T)
Reference rs281860485(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239014T>A
CLNSRC
CLNACC