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rs281860572

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860572(C;T)
Make rs281860572(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270227
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860572
ebirs281860572
HLIrs281860572
Exacrs281860572
Varsomers281860572
Maprs281860572
PheGenIrs281860572
hapmaprs281860572
1000 genomesrs281860572
hgdprs281860572
ensemblrs281860572
gopubmedrs281860572
geneviewrs281860572
scholarrs281860572
googlers281860572
pharmgkbrs281860572
gwascentralrs281860572
openSNPrs281860572
23andMers281860572
23andMe allrs281860572
SNP Nexus

SNPshotrs281860572
SNPdbers281860572
MSV3drs281860572
GWAS Ctlgrs281860572
Max Magnitude0
ClinVar
Risk rs281860572(T;T)
Alt rs281860572(T;T)
Reference rs281860572(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238004G>A
CLNSRC
CLNACC