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rs281860539

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860539(C;G)
Make rs281860539(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271106
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860539
ebirs281860539
HLIrs281860539
Exacrs281860539
Varsomers281860539
Maprs281860539
PheGenIrs281860539
hapmaprs281860539
1000 genomesrs281860539
hgdprs281860539
ensemblrs281860539
gopubmedrs281860539
geneviewrs281860539
scholarrs281860539
googlers281860539
pharmgkbrs281860539
gwascentralrs281860539
openSNPrs281860539
23andMers281860539
23andMe allrs281860539
SNP Nexus

SNPshotrs281860539
SNPdbers281860539
MSV3drs281860539
GWAS Ctlgrs281860539
Max Magnitude0
ClinVar
Risk rs281860539(G,T;G,T)
Alt rs281860539(G,T;G,T)
Reference rs281860539(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238883G>A; NC_000006.11:g.31238883G>C
CLNSRC
CLNACC