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rs281860473

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860473(C;T)
Make rs281860473(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271260
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860473
ebirs281860473
HLIrs281860473
Exacrs281860473
Varsomers281860473
Maprs281860473
PheGenIrs281860473
hapmaprs281860473
1000 genomesrs281860473
hgdprs281860473
ensemblrs281860473
gopubmedrs281860473
geneviewrs281860473
scholarrs281860473
googlers281860473
pharmgkbrs281860473
gwascentralrs281860473
openSNPrs281860473
23andMers281860473
23andMe allrs281860473
SNP Nexus

SNPshotrs281860473
SNPdbers281860473
MSV3drs281860473
GWAS Ctlgrs281860473
Max Magnitude0
ClinVar
Risk rs281860473(T;T)
Alt rs281860473(T;T)
Reference rs281860473(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239037G>A
CLNSRC
CLNACC