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rs281860557

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860557(C;T)
Make rs281860557(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270409
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860557
ebirs281860557
HLIrs281860557
Exacrs281860557
Varsomers281860557
Maprs281860557
PheGenIrs281860557
hapmaprs281860557
1000 genomesrs281860557
hgdprs281860557
ensemblrs281860557
gopubmedrs281860557
geneviewrs281860557
scholarrs281860557
googlers281860557
pharmgkbrs281860557
gwascentralrs281860557
openSNPrs281860557
23andMers281860557
23andMe allrs281860557
SNP Nexus

SNPshotrs281860557
SNPdbers281860557
MSV3drs281860557
GWAS Ctlgrs281860557
Max Magnitude0
ClinVar
Risk rs281860557(T;T)
Alt rs281860557(T;T)
Reference rs281860557(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238186G>A
CLNSRC
CLNACC