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rs281860420

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860420(C;T)
Make rs281860420(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271626
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860420
ebirs281860420
HLIrs281860420
Exacrs281860420
Varsomers281860420
Maprs281860420
PheGenIrs281860420
hapmaprs281860420
1000 genomesrs281860420
hgdprs281860420
ensemblrs281860420
gopubmedrs281860420
geneviewrs281860420
scholarrs281860420
googlers281860420
pharmgkbrs281860420
gwascentralrs281860420
openSNPrs281860420
23andMers281860420
23andMe allrs281860420
SNP Nexus

SNPshotrs281860420
SNPdbers281860420
MSV3drs281860420
GWAS Ctlgrs281860420
Max Magnitude0
ClinVar
Risk rs281860420(T;T)
Alt rs281860420(T;T)
Reference rs281860420(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239403G>A
CLNSRC
CLNACC