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rs281860504

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860504(C;G)
Make rs281860504(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271185
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860504
ebirs281860504
HLIrs281860504
Exacrs281860504
Varsomers281860504
Maprs281860504
PheGenIrs281860504
hapmaprs281860504
1000 genomesrs281860504
hgdprs281860504
ensemblrs281860504
gopubmedrs281860504
geneviewrs281860504
scholarrs281860504
googlers281860504
pharmgkbrs281860504
gwascentralrs281860504
openSNPrs281860504
23andMers281860504
23andMe allrs281860504
SNP Nexus

SNPshotrs281860504
SNPdbers281860504
MSV3drs281860504
GWAS Ctlgrs281860504
Max Magnitude0
ClinVar
Risk rs281860504(G;G)
Alt rs281860504(G;G)
Reference rs281860504(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238962G>C
CLNSRC
CLNACC