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rs281860483

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860483(C;T)
Make rs281860483(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271244
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860483
ebirs281860483
HLIrs281860483
Exacrs281860483
Varsomers281860483
Maprs281860483
PheGenIrs281860483
hapmaprs281860483
1000 genomesrs281860483
hgdprs281860483
ensemblrs281860483
gopubmedrs281860483
geneviewrs281860483
scholarrs281860483
googlers281860483
pharmgkbrs281860483
gwascentralrs281860483
openSNPrs281860483
23andMers281860483
23andMe allrs281860483
SNP Nexus

SNPshotrs281860483
SNPdbers281860483
MSV3drs281860483
GWAS Ctlgrs281860483
Max Magnitude0
ClinVar
Risk rs281860483(T;T)
Alt rs281860483(T;T)
Reference rs281860483(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239021G>A
CLNSRC
CLNACC