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rs281860465

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860465(A;A)
Make rs281860465(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271288
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860465
ebirs281860465
HLIrs281860465
Exacrs281860465
Varsomers281860465
Maprs281860465
PheGenIrs281860465
hapmaprs281860465
1000 genomesrs281860465
hgdprs281860465
ensemblrs281860465
gopubmedrs281860465
geneviewrs281860465
scholarrs281860465
googlers281860465
pharmgkbrs281860465
gwascentralrs281860465
openSNPrs281860465
23andMers281860465
23andMe allrs281860465
SNP Nexus

SNPshotrs281860465
SNPdbers281860465
MSV3drs281860465
GWAS Ctlgrs281860465
Max Magnitude0
ClinVar
Risk rs281860465(A,T;A,T)
Alt rs281860465(A,T;A,T)
Reference rs281860465(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239065C>A; NC_000006.11:g.31239065C>T
CLNSRC
CLNACC