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rs281860424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860424(C;T)
Make rs281860424(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271618
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860424
ebirs281860424
HLIrs281860424
Exacrs281860424
Varsomers281860424
Maprs281860424
PheGenIrs281860424
hapmaprs281860424
1000 genomesrs281860424
hgdprs281860424
ensemblrs281860424
gopubmedrs281860424
geneviewrs281860424
scholarrs281860424
googlers281860424
pharmgkbrs281860424
gwascentralrs281860424
openSNPrs281860424
23andMers281860424
23andMe allrs281860424
SNP Nexus

SNPshotrs281860424
SNPdbers281860424
MSV3drs281860424
GWAS Ctlgrs281860424
Max Magnitude0
ClinVar
Risk rs281860424(T;T)
Alt rs281860424(T;T)
Reference rs281860424(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239395G>A
CLNSRC
CLNACC