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rs281860427

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860427(A;A)
Make rs281860427(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271612
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860427
ebirs281860427
HLIrs281860427
Exacrs281860427
Varsomers281860427
Maprs281860427
PheGenIrs281860427
hapmaprs281860427
1000 genomesrs281860427
hgdprs281860427
ensemblrs281860427
gopubmedrs281860427
geneviewrs281860427
scholarrs281860427
googlers281860427
pharmgkbrs281860427
gwascentralrs281860427
openSNPrs281860427
23andMers281860427
23andMe allrs281860427
SNP Nexus

SNPshotrs281860427
SNPdbers281860427
MSV3drs281860427
GWAS Ctlgrs281860427
Max Magnitude0
ClinVar
Risk rs281860427(A,T;A,T)
Alt rs281860427(A,T;A,T)
Reference rs281860427(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239389G>A; NC_000006.11:g.31239389G>T
CLNSRC
CLNACC