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rs281860534

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860534(G;T)
Make rs281860534(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271119
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860534
ebirs281860534
HLIrs281860534
Exacrs281860534
Varsomers281860534
Maprs281860534
PheGenIrs281860534
hapmaprs281860534
1000 genomesrs281860534
hgdprs281860534
ensemblrs281860534
gopubmedrs281860534
geneviewrs281860534
scholarrs281860534
googlers281860534
pharmgkbrs281860534
gwascentralrs281860534
openSNPrs281860534
23andMers281860534
23andMe allrs281860534
SNP Nexus

SNPshotrs281860534
SNPdbers281860534
MSV3drs281860534
GWAS Ctlgrs281860534
Max Magnitude0
ClinVar
Risk rs281860534(T;T)
Alt rs281860534(T;T)
Reference rs281860534(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238896C>A
CLNSRC
CLNACC