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rs281860469

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860469(A;G)
Make rs281860469(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271276
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860469
ebirs281860469
HLIrs281860469
Exacrs281860469
Varsomers281860469
Maprs281860469
PheGenIrs281860469
hapmaprs281860469
1000 genomesrs281860469
hgdprs281860469
ensemblrs281860469
gopubmedrs281860469
geneviewrs281860469
scholarrs281860469
googlers281860469
pharmgkbrs281860469
gwascentralrs281860469
openSNPrs281860469
23andMers281860469
23andMe allrs281860469
SNP Nexus

SNPshotrs281860469
SNPdbers281860469
MSV3drs281860469
GWAS Ctlgrs281860469
Max Magnitude0
ClinVar
Risk rs281860469(G;G)
Alt rs281860469(G;G)
Reference rs281860469(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239053T>C
CLNSRC
CLNACC