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rs281860560

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860560(C;C)
Make rs281860560(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270373
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860560
ebirs281860560
HLIrs281860560
Exacrs281860560
Varsomers281860560
Maprs281860560
PheGenIrs281860560
hapmaprs281860560
1000 genomesrs281860560
hgdprs281860560
ensemblrs281860560
gopubmedrs281860560
geneviewrs281860560
scholarrs281860560
googlers281860560
pharmgkbrs281860560
gwascentralrs281860560
openSNPrs281860560
23andMers281860560
23andMe allrs281860560
SNP Nexus

SNPshotrs281860560
SNPdbers281860560
MSV3drs281860560
GWAS Ctlgrs281860560
Max Magnitude0
ClinVar
Risk rs281860560(C;C)
Alt rs281860560(C;C)
Reference rs281860560(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238150A>G
CLNSRC
CLNACC