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rs281860526

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860526(-;-)
Make rs281860526(-;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271128
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860526
ebirs281860526
HLIrs281860526
Exacrs281860526
Varsomers281860526
Maprs281860526
PheGenIrs281860526
hapmaprs281860526
1000 genomesrs281860526
hgdprs281860526
ensemblrs281860526
gopubmedrs281860526
geneviewrs281860526
scholarrs281860526
googlers281860526
pharmgkbrs281860526
gwascentralrs281860526
openSNPrs281860526
23andMers281860526
23andMe allrs281860526
SNP Nexus

SNPshotrs281860526
SNPdbers281860526
MSV3drs281860526
GWAS Ctlgrs281860526
Max Magnitude0
ClinVar
Risk rs281860526(;)
Alt rs281860526(;)
Reference rs281860526(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238905delG
CLNSRC
CLNACC