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rs281860458

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860458(C;C)
Make rs281860458(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271300
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860458
ebirs281860458
HLIrs281860458
Exacrs281860458
Varsomers281860458
Maprs281860458
PheGenIrs281860458
hapmaprs281860458
1000 genomesrs281860458
hgdprs281860458
ensemblrs281860458
gopubmedrs281860458
geneviewrs281860458
scholarrs281860458
googlers281860458
pharmgkbrs281860458
gwascentralrs281860458
openSNPrs281860458
23andMers281860458
23andMe allrs281860458
SNP Nexus

SNPshotrs281860458
SNPdbers281860458
MSV3drs281860458
GWAS Ctlgrs281860458
Max Magnitude0
ClinVar
Risk rs281860458(C;C)
Alt rs281860458(C;C)
Reference rs281860458(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239077C>G
CLNSRC
CLNACC