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

rs281860456

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860456(A;A)
Make rs281860456(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271309
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860456
ebirs281860456
HLIrs281860456
Exacrs281860456
Varsomers281860456
Maprs281860456
PheGenIrs281860456
hapmaprs281860456
1000 genomesrs281860456
hgdprs281860456
ensemblrs281860456
gopubmedrs281860456
geneviewrs281860456
scholarrs281860456
googlers281860456
pharmgkbrs281860456
gwascentralrs281860456
openSNPrs281860456
23andMers281860456
23andMe allrs281860456
SNP Nexus

SNPshotrs281860456
SNPdbers281860456
MSV3drs281860456
GWAS Ctlgrs281860456
Max Magnitude0
ClinVar
Risk rs281860456(A,C;A,C)
Alt rs281860456(A,C;A,C)
Reference rs281860456(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239086C>G; NC_000006.11:g.31239086C>T
CLNSRC
CLNACC