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rs281860556

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860556(C;C)
Make rs281860556(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270411
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860556
ebirs281860556
HLIrs281860556
Exacrs281860556
Varsomers281860556
Maprs281860556
PheGenIrs281860556
hapmaprs281860556
1000 genomesrs281860556
hgdprs281860556
ensemblrs281860556
gopubmedrs281860556
geneviewrs281860556
scholarrs281860556
googlers281860556
pharmgkbrs281860556
gwascentralrs281860556
openSNPrs281860556
23andMers281860556
23andMe allrs281860556
SNP Nexus

SNPshotrs281860556
SNPdbers281860556
MSV3drs281860556
GWAS Ctlgrs281860556
Max Magnitude0
ClinVar
Risk rs281860556(C;C)
Alt rs281860556(C;C)
Reference rs281860556(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238188A>G
CLNSRC
CLNACC