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rs281860585

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860585(-;-)
Make rs281860585(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269808
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860585
ebirs281860585
HLIrs281860585
Exacrs281860585
Varsomers281860585
Maprs281860585
PheGenIrs281860585
hapmaprs281860585
1000 genomesrs281860585
hgdprs281860585
ensemblrs281860585
gopubmedrs281860585
geneviewrs281860585
scholarrs281860585
googlers281860585
pharmgkbrs281860585
gwascentralrs281860585
openSNPrs281860585
23andMers281860585
23andMe allrs281860585
SNP Nexus

SNPshotrs281860585
SNPdbers281860585
MSV3drs281860585
GWAS Ctlgrs281860585
Max Magnitude0
ClinVar
Risk rs281860585(;)
Alt rs281860585(;)
Reference rs281860585(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237585delT
CLNSRC
CLNACC