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rs281860521

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860521(G;G)
Make rs281860521(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271141
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860521
ebirs281860521
HLIrs281860521
Exacrs281860521
Varsomers281860521
Maprs281860521
PheGenIrs281860521
hapmaprs281860521
1000 genomesrs281860521
hgdprs281860521
ensemblrs281860521
gopubmedrs281860521
geneviewrs281860521
scholarrs281860521
googlers281860521
pharmgkbrs281860521
gwascentralrs281860521
openSNPrs281860521
23andMers281860521
23andMe allrs281860521
SNP Nexus

SNPshotrs281860521
SNPdbers281860521
MSV3drs281860521
GWAS Ctlgrs281860521
Max Magnitude0
ClinVar
Risk rs281860521(G;G)
Alt rs281860521(G;G)
Reference rs281860521(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238918A>C
CLNSRC
CLNACC