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rs281860565

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860565(C;T)
Make rs281860565(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270352
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860565
ebirs281860565
HLIrs281860565
Exacrs281860565
Varsomers281860565
Maprs281860565
PheGenIrs281860565
hapmaprs281860565
1000 genomesrs281860565
hgdprs281860565
ensemblrs281860565
gopubmedrs281860565
geneviewrs281860565
scholarrs281860565
googlers281860565
pharmgkbrs281860565
gwascentralrs281860565
openSNPrs281860565
23andMers281860565
23andMe allrs281860565
SNP Nexus

SNPshotrs281860565
SNPdbers281860565
MSV3drs281860565
GWAS Ctlgrs281860565
Max Magnitude0
ClinVar
Risk rs281860565(T;T)
Alt rs281860565(T;T)
Reference rs281860565(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238129G>A
CLNSRC
CLNACC