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rs281860517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860517(C;C)
Make rs281860517(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271150
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860517
ebirs281860517
HLIrs281860517
Exacrs281860517
Varsomers281860517
Maprs281860517
PheGenIrs281860517
hapmaprs281860517
1000 genomesrs281860517
hgdprs281860517
ensemblrs281860517
gopubmedrs281860517
geneviewrs281860517
scholarrs281860517
googlers281860517
pharmgkbrs281860517
gwascentralrs281860517
openSNPrs281860517
23andMers281860517
23andMe allrs281860517
SNP Nexus

SNPshotrs281860517
SNPdbers281860517
MSV3drs281860517
GWAS Ctlgrs281860517
Max Magnitude0
ClinVar
Risk rs281860517(C;C)
Alt rs281860517(C;C)
Reference rs281860517(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238927C>G
CLNSRC
CLNACC