Have questions? Visit https://www.reddit.com/r/SNPedia

rs281860409

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860409(C;C)
Make rs281860409(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271650
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860409
ebirs281860409
HLIrs281860409
Exacrs281860409
Varsomers281860409
Maprs281860409
PheGenIrs281860409
hapmaprs281860409
1000 genomesrs281860409
hgdprs281860409
ensemblrs281860409
gopubmedrs281860409
geneviewrs281860409
scholarrs281860409
googlers281860409
pharmgkbrs281860409
gwascentralrs281860409
openSNPrs281860409
23andMers281860409
23andMe allrs281860409
SNP Nexus

SNPshotrs281860409
SNPdbers281860409
MSV3drs281860409
GWAS Ctlgrs281860409
Max Magnitude0
ClinVar
Risk rs281860409(C;C)
Alt rs281860409(C;C)
Reference rs281860409(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239427C>G
CLNSRC
CLNACC