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rs281860575

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860575(-;-)
Make rs281860575(-;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270141
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860575
ebirs281860575
HLIrs281860575
Exacrs281860575
Varsomers281860575
Maprs281860575
PheGenIrs281860575
hapmaprs281860575
1000 genomesrs281860575
hgdprs281860575
ensemblrs281860575
gopubmedrs281860575
geneviewrs281860575
scholarrs281860575
googlers281860575
pharmgkbrs281860575
gwascentralrs281860575
openSNPrs281860575
23andMers281860575
23andMe allrs281860575
SNP Nexus

SNPshotrs281860575
SNPdbers281860575
MSV3drs281860575
GWAS Ctlgrs281860575
Max Magnitude0
ClinVar
Risk rs281860575(;)
Alt rs281860575(;)
Reference rs281860575(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237918delG
CLNSRC
CLNACC