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rs281860478

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860478(A;T)
Make rs281860478(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271252
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860478
ebirs281860478
HLIrs281860478
Exacrs281860478
Varsomers281860478
Maprs281860478
PheGenIrs281860478
hapmaprs281860478
1000 genomesrs281860478
hgdprs281860478
ensemblrs281860478
gopubmedrs281860478
geneviewrs281860478
scholarrs281860478
googlers281860478
pharmgkbrs281860478
gwascentralrs281860478
openSNPrs281860478
23andMers281860478
23andMe allrs281860478
SNP Nexus

SNPshotrs281860478
SNPdbers281860478
MSV3drs281860478
GWAS Ctlgrs281860478
Max Magnitude0
ClinVar
Risk rs281860478(T;T)
Alt rs281860478(T;T)
Reference rs281860478(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239029T>A
CLNSRC
CLNACC