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rs281860475

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860475(A;A)
Make rs281860475(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271256
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860475
ebirs281860475
HLIrs281860475
Exacrs281860475
Varsomers281860475
Maprs281860475
PheGenIrs281860475
hapmaprs281860475
1000 genomesrs281860475
hgdprs281860475
ensemblrs281860475
gopubmedrs281860475
geneviewrs281860475
scholarrs281860475
googlers281860475
pharmgkbrs281860475
gwascentralrs281860475
openSNPrs281860475
23andMers281860475
23andMe allrs281860475
SNP Nexus

SNPshotrs281860475
SNPdbers281860475
MSV3drs281860475
GWAS Ctlgrs281860475
Max Magnitude0
ClinVar
Risk rs281860475(A;A)
Alt rs281860475(A;A)
Reference rs281860475(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239033C>T
CLNSRC
CLNACC