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rs281860470

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860470(C;T)
Make rs281860470(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271270
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860470
ebirs281860470
HLIrs281860470
Exacrs281860470
Varsomers281860470
Maprs281860470
PheGenIrs281860470
hapmaprs281860470
1000 genomesrs281860470
hgdprs281860470
ensemblrs281860470
gopubmedrs281860470
geneviewrs281860470
scholarrs281860470
googlers281860470
pharmgkbrs281860470
gwascentralrs281860470
openSNPrs281860470
23andMers281860470
23andMe allrs281860470
SNP Nexus

SNPshotrs281860470
SNPdbers281860470
MSV3drs281860470
GWAS Ctlgrs281860470
Max Magnitude0
ClinVar
Risk rs281860470(T;T)
Alt rs281860470(T;T)
Reference rs281860470(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239047G>A
CLNSRC
CLNACC