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rs281860591

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860591(-;-)
Make rs281860591(-;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269398
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860591
ebirs281860591
HLIrs281860591
Exacrs281860591
Varsomers281860591
Maprs281860591
PheGenIrs281860591
hapmaprs281860591
1000 genomesrs281860591
hgdprs281860591
ensemblrs281860591
gopubmedrs281860591
geneviewrs281860591
scholarrs281860591
googlers281860591
pharmgkbrs281860591
gwascentralrs281860591
openSNPrs281860591
23andMers281860591
23andMe allrs281860591
SNP Nexus

SNPshotrs281860591
SNPdbers281860591
MSV3drs281860591
GWAS Ctlgrs281860591
Max Magnitude0
ClinVar
Risk rs281860591(;)
Alt rs281860591(;)
Reference rs281860591(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237175delA
CLNSRC
CLNACC