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rs281860503

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860503(A;A)
Make rs281860503(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271187
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860503
ebirs281860503
HLIrs281860503
Exacrs281860503
Varsomers281860503
Maprs281860503
PheGenIrs281860503
hapmaprs281860503
1000 genomesrs281860503
hgdprs281860503
ensemblrs281860503
gopubmedrs281860503
geneviewrs281860503
scholarrs281860503
googlers281860503
pharmgkbrs281860503
gwascentralrs281860503
openSNPrs281860503
23andMers281860503
23andMe allrs281860503
SNP Nexus

SNPshotrs281860503
SNPdbers281860503
MSV3drs281860503
GWAS Ctlgrs281860503
Max Magnitude0
ClinVar
Risk rs281860503(A,G,T;A,G,T)
Alt rs281860503(A,G,T;A,G,T)
Reference rs281860503(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238964G>A; NC_000006.11:g.31238964G>C; NC_000006.11:g.31238964G>T
CLNSRC
CLNACC