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rs281860520

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860520(A;A)
Make rs281860520(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271143
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860520
ebirs281860520
HLIrs281860520
Exacrs281860520
Varsomers281860520
Maprs281860520
PheGenIrs281860520
hapmaprs281860520
1000 genomesrs281860520
hgdprs281860520
ensemblrs281860520
gopubmedrs281860520
geneviewrs281860520
scholarrs281860520
googlers281860520
pharmgkbrs281860520
gwascentralrs281860520
openSNPrs281860520
23andMers281860520
23andMe allrs281860520
SNP Nexus

SNPshotrs281860520
SNPdbers281860520
MSV3drs281860520
GWAS Ctlgrs281860520
Max Magnitude0
ClinVar
Risk rs281860520(A,T;A,T)
Alt rs281860520(A,T;A,T)
Reference rs281860520(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238920G>A; NC_000006.11:g.31238920G>T
CLNSRC
CLNACC