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

rs281860411

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860411(A;A)
Make rs281860411(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271642
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860411
ebirs281860411
HLIrs281860411
Exacrs281860411
Varsomers281860411
Maprs281860411
PheGenIrs281860411
hapmaprs281860411
1000 genomesrs281860411
hgdprs281860411
ensemblrs281860411
gopubmedrs281860411
geneviewrs281860411
scholarrs281860411
googlers281860411
pharmgkbrs281860411
gwascentralrs281860411
openSNPrs281860411
23andMers281860411
23andMe allrs281860411
SNP Nexus

SNPshotrs281860411
SNPdbers281860411
MSV3drs281860411
GWAS Ctlgrs281860411
Max Magnitude0
ClinVar
Risk rs281860411(A,T;A,T)
Alt rs281860411(A,T;A,T)
Reference rs281860411(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239419C>A; NC_000006.11:g.31239419C>T
CLNSRC
CLNACC