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rs281860450

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860450(A;A)
Make rs281860450(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271321
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860450
ebirs281860450
HLIrs281860450
Exacrs281860450
Varsomers281860450
Maprs281860450
PheGenIrs281860450
hapmaprs281860450
1000 genomesrs281860450
hgdprs281860450
ensemblrs281860450
gopubmedrs281860450
geneviewrs281860450
scholarrs281860450
googlers281860450
pharmgkbrs281860450
gwascentralrs281860450
openSNPrs281860450
23andMers281860450
23andMe allrs281860450
SNP Nexus

SNPshotrs281860450
SNPdbers281860450
MSV3drs281860450
GWAS Ctlgrs281860450
Max Magnitude0
ClinVar
Risk rs281860450(A;A)
Alt rs281860450(A;A)
Reference rs281860450(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239098C>T
CLNSRC
CLNACC