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rs281860564

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860564(C;T)
Make rs281860564(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270359
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860564
ebirs281860564
HLIrs281860564
Exacrs281860564
Varsomers281860564
Maprs281860564
PheGenIrs281860564
hapmaprs281860564
1000 genomesrs281860564
hgdprs281860564
ensemblrs281860564
gopubmedrs281860564
geneviewrs281860564
scholarrs281860564
googlers281860564
pharmgkbrs281860564
gwascentralrs281860564
openSNPrs281860564
23andMers281860564
23andMe allrs281860564
SNP Nexus

SNPshotrs281860564
SNPdbers281860564
MSV3drs281860564
GWAS Ctlgrs281860564
Max Magnitude0
ClinVar
Risk rs281860564(T;T)
Alt rs281860564(T;T)
Reference rs281860564(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238136G>A
CLNSRC
CLNACC