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rs281860438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860438(C;T)
Make rs281860438(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271485
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860438
ebirs281860438
HLIrs281860438
Exacrs281860438
Varsomers281860438
Maprs281860438
PheGenIrs281860438
hapmaprs281860438
1000 genomesrs281860438
hgdprs281860438
ensemblrs281860438
gopubmedrs281860438
geneviewrs281860438
scholarrs281860438
googlers281860438
pharmgkbrs281860438
gwascentralrs281860438
openSNPrs281860438
23andMers281860438
23andMe allrs281860438
SNP Nexus

SNPshotrs281860438
SNPdbers281860438
MSV3drs281860438
GWAS Ctlgrs281860438
Max Magnitude0
ClinVar
Risk rs281860438(T;T)
Alt rs281860438(T;T)
Reference rs281860438(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239262G>A
CLNSRC
CLNACC