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rs281860553

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860553(A;C)
Make rs281860553(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270443
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860553
ebirs281860553
HLIrs281860553
Exacrs281860553
Varsomers281860553
Maprs281860553
PheGenIrs281860553
hapmaprs281860553
1000 genomesrs281860553
hgdprs281860553
ensemblrs281860553
gopubmedrs281860553
geneviewrs281860553
scholarrs281860553
googlers281860553
pharmgkbrs281860553
gwascentralrs281860553
openSNPrs281860553
23andMers281860553
23andMe allrs281860553
SNP Nexus

SNPshotrs281860553
SNPdbers281860553
MSV3drs281860553
GWAS Ctlgrs281860553
Max Magnitude0
ClinVar
Risk rs281860553(C,G;C,G)
Alt rs281860553(C,G;C,G)
Reference rs281860553(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238220T>C; NC_000006.11:g.31238220T>G
CLNSRC
CLNACC