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rs281860532

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860532(A;T)
Make rs281860532(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271123
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860532
ebirs281860532
HLIrs281860532
Exacrs281860532
Varsomers281860532
Maprs281860532
PheGenIrs281860532
hapmaprs281860532
1000 genomesrs281860532
hgdprs281860532
ensemblrs281860532
gopubmedrs281860532
geneviewrs281860532
scholarrs281860532
googlers281860532
pharmgkbrs281860532
gwascentralrs281860532
openSNPrs281860532
23andMers281860532
23andMe allrs281860532
SNP Nexus

SNPshotrs281860532
SNPdbers281860532
MSV3drs281860532
GWAS Ctlgrs281860532
Max Magnitude0
ClinVar
Risk rs281860532(T;T)
Alt rs281860532(T;T)
Reference rs281860532(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238900T>A
CLNSRC
CLNACC