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rs281860554

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860554(A;G)
Make rs281860554(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270435
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860554
ebirs281860554
HLIrs281860554
Exacrs281860554
Varsomers281860554
Maprs281860554
PheGenIrs281860554
hapmaprs281860554
1000 genomesrs281860554
hgdprs281860554
ensemblrs281860554
gopubmedrs281860554
geneviewrs281860554
scholarrs281860554
googlers281860554
pharmgkbrs281860554
gwascentralrs281860554
openSNPrs281860554
23andMers281860554
23andMe allrs281860554
SNP Nexus

SNPshotrs281860554
SNPdbers281860554
MSV3drs281860554
GWAS Ctlgrs281860554
Max Magnitude0
ClinVar
Risk rs281860554(G;G)
Alt rs281860554(G;G)
Reference rs281860554(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238212T>C
CLNSRC
CLNACC