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rs281860551

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860551(C;T)
Make rs281860551(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270454
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860551
ebirs281860551
HLIrs281860551
Exacrs281860551
Varsomers281860551
Maprs281860551
PheGenIrs281860551
hapmaprs281860551
1000 genomesrs281860551
hgdprs281860551
ensemblrs281860551
gopubmedrs281860551
geneviewrs281860551
scholarrs281860551
googlers281860551
pharmgkbrs281860551
gwascentralrs281860551
openSNPrs281860551
23andMers281860551
23andMe allrs281860551
SNP Nexus

SNPshotrs281860551
SNPdbers281860551
MSV3drs281860551
GWAS Ctlgrs281860551
Max Magnitude0
ClinVar
Risk rs281860551(T;T)
Alt rs281860551(T;T)
Reference rs281860551(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238231G>A
CLNSRC
CLNACC