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rs281860495

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860495(A;A)
Make rs281860495(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271204
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860495
ebirs281860495
HLIrs281860495
Exacrs281860495
Varsomers281860495
Maprs281860495
PheGenIrs281860495
hapmaprs281860495
1000 genomesrs281860495
hgdprs281860495
ensemblrs281860495
gopubmedrs281860495
geneviewrs281860495
scholarrs281860495
googlers281860495
pharmgkbrs281860495
gwascentralrs281860495
openSNPrs281860495
23andMers281860495
23andMe allrs281860495
SNP Nexus

SNPshotrs281860495
SNPdbers281860495
MSV3drs281860495
GWAS Ctlgrs281860495
Max Magnitude0
ClinVar
Risk rs281860495(A,T;A,T)
Alt rs281860495(A,T;A,T)
Reference rs281860495(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238981G>A; NC_000006.11:g.31238981G>T
CLNSRC
CLNACC