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rs281860455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860455(A;A)
Make rs281860455(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271310
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860455
ebirs281860455
HLIrs281860455
Exacrs281860455
Varsomers281860455
Maprs281860455
PheGenIrs281860455
hapmaprs281860455
1000 genomesrs281860455
hgdprs281860455
ensemblrs281860455
gopubmedrs281860455
geneviewrs281860455
scholarrs281860455
googlers281860455
pharmgkbrs281860455
gwascentralrs281860455
openSNPrs281860455
23andMers281860455
23andMe allrs281860455
SNP Nexus

SNPshotrs281860455
SNPdbers281860455
MSV3drs281860455
GWAS Ctlgrs281860455
Max Magnitude0
ClinVar
Risk rs281860455(A;A)
Alt rs281860455(A;A)
Reference rs281860455(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239087C>T
CLNSRC
CLNACC