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rs281860587

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs281860587(-;-)
Make rs281860587(-;TG)
Make rs281860587(TG;TG)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269799
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860587
ebirs281860587
HLIrs281860587
Exacrs281860587
Varsomers281860587
Maprs281860587
PheGenIrs281860587
hapmaprs281860587
1000 genomesrs281860587
hgdprs281860587
ensemblrs281860587
gopubmedrs281860587
geneviewrs281860587
scholarrs281860587
googlers281860587
pharmgkbrs281860587
gwascentralrs281860587
openSNPrs281860587
23andMers281860587
23andMe allrs281860587
SNP Nexus

SNPshotrs281860587
SNPdbers281860587
MSV3drs281860587
GWAS Ctlgrs281860587
Max Magnitude0
ClinVar
Risk rs281860587(TG;TG)
Alt rs281860587(TG;TG)
Reference rs281860587(;)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237576_31237577insCA
CLNSRC
CLNACC