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rs281860536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860536(C;G)
Make rs281860536(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271113
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860536
ebirs281860536
HLIrs281860536
Exacrs281860536
Varsomers281860536
Maprs281860536
PheGenIrs281860536
hapmaprs281860536
1000 genomesrs281860536
hgdprs281860536
ensemblrs281860536
gopubmedrs281860536
geneviewrs281860536
scholarrs281860536
googlers281860536
pharmgkbrs281860536
gwascentralrs281860536
openSNPrs281860536
23andMers281860536
23andMe allrs281860536
SNP Nexus

SNPshotrs281860536
SNPdbers281860536
MSV3drs281860536
GWAS Ctlgrs281860536
Max Magnitude0
ClinVar
Risk rs281860536(G;G)
Alt rs281860536(G;G)
Reference rs281860536(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238890G>C
CLNSRC
CLNACC