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rs281860454

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860454(G;T)
Make rs281860454(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271311
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860454
ebirs281860454
HLIrs281860454
Exacrs281860454
Varsomers281860454
Maprs281860454
PheGenIrs281860454
hapmaprs281860454
1000 genomesrs281860454
hgdprs281860454
ensemblrs281860454
gopubmedrs281860454
geneviewrs281860454
scholarrs281860454
googlers281860454
pharmgkbrs281860454
gwascentralrs281860454
openSNPrs281860454
23andMers281860454
23andMe allrs281860454
SNP Nexus

SNPshotrs281860454
SNPdbers281860454
MSV3drs281860454
GWAS Ctlgrs281860454
Max Magnitude0
ClinVar
Risk rs281860454(T;T)
Alt rs281860454(T;T)
Reference rs281860454(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239088C>A
CLNSRC
CLNACC