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rs281860421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860421(A;A)
Make rs281860421(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271625
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860421
ebirs281860421
HLIrs281860421
Exacrs281860421
Varsomers281860421
Maprs281860421
PheGenIrs281860421
hapmaprs281860421
1000 genomesrs281860421
hgdprs281860421
ensemblrs281860421
gopubmedrs281860421
geneviewrs281860421
scholarrs281860421
googlers281860421
pharmgkbrs281860421
gwascentralrs281860421
openSNPrs281860421
23andMers281860421
23andMe allrs281860421
SNP Nexus

SNPshotrs281860421
SNPdbers281860421
MSV3drs281860421
GWAS Ctlgrs281860421
Max Magnitude0
ClinVar
Risk rs281860421(A,T;A,T)
Alt rs281860421(A,T;A,T)
Reference rs281860421(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239402C>A; NC_000006.11:g.31239402C>T
CLNSRC
CLNACC