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rs281860444

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860444(A;G)
Make rs281860444(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271333
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860444
ebirs281860444
HLIrs281860444
Exacrs281860444
Varsomers281860444
Maprs281860444
PheGenIrs281860444
hapmaprs281860444
1000 genomesrs281860444
hgdprs281860444
ensemblrs281860444
gopubmedrs281860444
geneviewrs281860444
scholarrs281860444
googlers281860444
pharmgkbrs281860444
gwascentralrs281860444
openSNPrs281860444
23andMers281860444
23andMe allrs281860444
SNP Nexus

SNPshotrs281860444
SNPdbers281860444
MSV3drs281860444
GWAS Ctlgrs281860444
Max Magnitude0
ClinVar
Risk rs281860444(G;G)
Alt rs281860444(G;G)
Reference rs281860444(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239110T>C
CLNSRC
CLNACC