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rs281860549

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860549(C;G)
Make rs281860549(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271075
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860549
ebirs281860549
HLIrs281860549
Exacrs281860549
Varsomers281860549
Maprs281860549
PheGenIrs281860549
hapmaprs281860549
1000 genomesrs281860549
hgdprs281860549
ensemblrs281860549
gopubmedrs281860549
geneviewrs281860549
scholarrs281860549
googlers281860549
pharmgkbrs281860549
gwascentralrs281860549
openSNPrs281860549
23andMers281860549
23andMe allrs281860549
SNP Nexus

SNPshotrs281860549
SNPdbers281860549
MSV3drs281860549
GWAS Ctlgrs281860549
Max Magnitude0
ClinVar
Risk rs281860549(G,T;G,T)
Alt rs281860549(G,T;G,T)
Reference rs281860549(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238852G>A; NC_000006.11:g.31238852G>C
CLNSRC
CLNACC