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

rs281860407

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860407(C;C)
Make rs281860407(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271654
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860407
ebirs281860407
HLIrs281860407
Exacrs281860407
Varsomers281860407
Maprs281860407
PheGenIrs281860407
hapmaprs281860407
1000 genomesrs281860407
hgdprs281860407
ensemblrs281860407
gopubmedrs281860407
geneviewrs281860407
scholarrs281860407
googlers281860407
pharmgkbrs281860407
gwascentralrs281860407
openSNPrs281860407
23andMers281860407
23andMe allrs281860407
SNP Nexus

SNPshotrs281860407
SNPdbers281860407
MSV3drs281860407
GWAS Ctlgrs281860407
Max Magnitude0
ClinVar
Risk rs281860407(C,T;C,T)
Alt rs281860407(C,T;C,T)
Reference rs281860407(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239431C>A; NC_000006.11:g.31239431C>G
CLNSRC
CLNACC