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rs281860505

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860505(A;T)
Make rs281860505(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271183
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860505
ebirs281860505
HLIrs281860505
Exacrs281860505
Varsomers281860505
Maprs281860505
PheGenIrs281860505
hapmaprs281860505
1000 genomesrs281860505
hgdprs281860505
ensemblrs281860505
gopubmedrs281860505
geneviewrs281860505
scholarrs281860505
googlers281860505
pharmgkbrs281860505
gwascentralrs281860505
openSNPrs281860505
23andMers281860505
23andMe allrs281860505
SNP Nexus

SNPshotrs281860505
SNPdbers281860505
MSV3drs281860505
GWAS Ctlgrs281860505
Max Magnitude0
ClinVar
Risk rs281860505(T;T)
Alt rs281860505(T;T)
Reference rs281860505(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238960T>A
CLNSRC
CLNACC