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rs281860479

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860479(C;G)
Make rs281860479(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271251
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860479
ebirs281860479
HLIrs281860479
Exacrs281860479
Varsomers281860479
Maprs281860479
PheGenIrs281860479
hapmaprs281860479
1000 genomesrs281860479
hgdprs281860479
ensemblrs281860479
gopubmedrs281860479
geneviewrs281860479
scholarrs281860479
googlers281860479
pharmgkbrs281860479
gwascentralrs281860479
openSNPrs281860479
23andMers281860479
23andMe allrs281860479
SNP Nexus

SNPshotrs281860479
SNPdbers281860479
MSV3drs281860479
GWAS Ctlgrs281860479
Max Magnitude0
ClinVar
Risk rs281860479(G,T;G,T)
Alt rs281860479(G,T;G,T)
Reference rs281860479(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239028G>A; NC_000006.11:g.31239028G>C
CLNSRC
CLNACC