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rs281860442

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860442(A;A)
Make rs281860442(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271341
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860442
ebirs281860442
HLIrs281860442
Exacrs281860442
Varsomers281860442
Maprs281860442
PheGenIrs281860442
hapmaprs281860442
1000 genomesrs281860442
hgdprs281860442
ensemblrs281860442
gopubmedrs281860442
geneviewrs281860442
scholarrs281860442
googlers281860442
pharmgkbrs281860442
gwascentralrs281860442
openSNPrs281860442
23andMers281860442
23andMe allrs281860442
SNP Nexus

SNPshotrs281860442
SNPdbers281860442
MSV3drs281860442
GWAS Ctlgrs281860442
Max Magnitude0
ClinVar
Risk rs281860442(A,T;A,T)
Alt rs281860442(A,T;A,T)
Reference rs281860442(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239118G>A; NC_000006.11:g.31239118G>T
CLNSRC
CLNACC