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rs281860523

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860523(C;C)
Make rs281860523(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271137
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860523
ebirs281860523
HLIrs281860523
Exacrs281860523
Varsomers281860523
Maprs281860523
PheGenIrs281860523
hapmaprs281860523
1000 genomesrs281860523
hgdprs281860523
ensemblrs281860523
gopubmedrs281860523
geneviewrs281860523
scholarrs281860523
googlers281860523
pharmgkbrs281860523
gwascentralrs281860523
openSNPrs281860523
23andMers281860523
23andMe allrs281860523
SNP Nexus

SNPshotrs281860523
SNPdbers281860523
MSV3drs281860523
GWAS Ctlgrs281860523
Max Magnitude0
ClinVar
Risk rs281860523(C;C)
Alt rs281860523(C;C)
Reference rs281860523(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238914C>G
CLNSRC
CLNACC