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rs281860569

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860569(C;T)
Make rs281860569(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270314
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860569
ebirs281860569
HLIrs281860569
Exacrs281860569
Varsomers281860569
Maprs281860569
PheGenIrs281860569
hapmaprs281860569
1000 genomesrs281860569
hgdprs281860569
ensemblrs281860569
gopubmedrs281860569
geneviewrs281860569
scholarrs281860569
googlers281860569
pharmgkbrs281860569
gwascentralrs281860569
openSNPrs281860569
23andMers281860569
23andMe allrs281860569
SNP Nexus

SNPshotrs281860569
SNPdbers281860569
MSV3drs281860569
GWAS Ctlgrs281860569
Max Magnitude0
ClinVar
Risk rs281860569(T;T)
Alt rs281860569(T;T)
Reference rs281860569(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238091G>A
CLNSRC
CLNACC