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rs281860464

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860464(C;T)
Make rs281860464(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271289
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860464
ebirs281860464
HLIrs281860464
Exacrs281860464
Varsomers281860464
Maprs281860464
PheGenIrs281860464
hapmaprs281860464
1000 genomesrs281860464
hgdprs281860464
ensemblrs281860464
gopubmedrs281860464
geneviewrs281860464
scholarrs281860464
googlers281860464
pharmgkbrs281860464
gwascentralrs281860464
openSNPrs281860464
23andMers281860464
23andMe allrs281860464
SNP Nexus

SNPshotrs281860464
SNPdbers281860464
MSV3drs281860464
GWAS Ctlgrs281860464
Max Magnitude0
ClinVar
Risk rs281860464(T;T)
Alt rs281860464(T;T)
Reference rs281860464(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239066G>A
CLNSRC
CLNACC