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rs281860509

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860509(A;G)
Make rs281860509(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271177
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860509
ebirs281860509
HLIrs281860509
Exacrs281860509
Varsomers281860509
Maprs281860509
PheGenIrs281860509
hapmaprs281860509
1000 genomesrs281860509
hgdprs281860509
ensemblrs281860509
gopubmedrs281860509
geneviewrs281860509
scholarrs281860509
googlers281860509
pharmgkbrs281860509
gwascentralrs281860509
openSNPrs281860509
23andMers281860509
23andMe allrs281860509
SNP Nexus

SNPshotrs281860509
SNPdbers281860509
MSV3drs281860509
GWAS Ctlgrs281860509
Max Magnitude0
ClinVar
Risk rs281860509(G;G)
Alt rs281860509(G;G)
Reference rs281860509(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238954T>C
CLNSRC
CLNACC