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rs281860439

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860439(-;-)
Make rs281860439(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271348
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860439
ebirs281860439
HLIrs281860439
Exacrs281860439
Varsomers281860439
Maprs281860439
PheGenIrs281860439
hapmaprs281860439
1000 genomesrs281860439
hgdprs281860439
ensemblrs281860439
gopubmedrs281860439
geneviewrs281860439
scholarrs281860439
googlers281860439
pharmgkbrs281860439
gwascentralrs281860439
openSNPrs281860439
23andMers281860439
23andMe allrs281860439
SNP Nexus

SNPshotrs281860439
SNPdbers281860439
MSV3drs281860439
GWAS Ctlgrs281860439
Max Magnitude0
ClinVar
Risk rs281860439(;)
Alt rs281860439(;)
Reference rs281860439(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239125delC
CLNSRC
CLNACC