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rs281860480

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860480(A;A)
Make rs281860480(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271249
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860480
ebirs281860480
HLIrs281860480
Exacrs281860480
Varsomers281860480
Maprs281860480
PheGenIrs281860480
hapmaprs281860480
1000 genomesrs281860480
hgdprs281860480
ensemblrs281860480
gopubmedrs281860480
geneviewrs281860480
scholarrs281860480
googlers281860480
pharmgkbrs281860480
gwascentralrs281860480
openSNPrs281860480
23andMers281860480
23andMe allrs281860480
SNP Nexus

SNPshotrs281860480
SNPdbers281860480
MSV3drs281860480
GWAS Ctlgrs281860480
Max Magnitude0
ClinVar
Risk rs281860480(A;A)
Alt rs281860480(A;A)
Reference rs281860480(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239026A>T
CLNSRC
CLNACC