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rs281860436

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860436(A;A)
Make rs281860436(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271600
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860436
ebirs281860436
HLIrs281860436
Exacrs281860436
Varsomers281860436
Maprs281860436
PheGenIrs281860436
hapmaprs281860436
1000 genomesrs281860436
hgdprs281860436
ensemblrs281860436
gopubmedrs281860436
geneviewrs281860436
scholarrs281860436
googlers281860436
pharmgkbrs281860436
gwascentralrs281860436
openSNPrs281860436
23andMers281860436
23andMe allrs281860436
SNP Nexus

SNPshotrs281860436
SNPdbers281860436
MSV3drs281860436
GWAS Ctlgrs281860436
Max Magnitude0
ClinVar
Risk rs281860436(A,T;A,T)
Alt rs281860436(A,T;A,T)
Reference rs281860436(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239377G>A; NC_000006.11:g.31239377G>T
CLNSRC
CLNACC