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

rs281860430

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860430(A;A)
Make rs281860430(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271609
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860430
ebirs281860430
HLIrs281860430
Exacrs281860430
Varsomers281860430
Maprs281860430
PheGenIrs281860430
hapmaprs281860430
1000 genomesrs281860430
hgdprs281860430
ensemblrs281860430
gopubmedrs281860430
geneviewrs281860430
scholarrs281860430
googlers281860430
pharmgkbrs281860430
gwascentralrs281860430
openSNPrs281860430
23andMers281860430
23andMe allrs281860430
SNP Nexus

SNPshotrs281860430
SNPdbers281860430
MSV3drs281860430
GWAS Ctlgrs281860430
Max Magnitude0
ClinVar
Risk rs281860430(A,C;A,C)
Alt rs281860430(A,C;A,C)
Reference rs281860430(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239386C>G; NC_000006.11:g.31239386C>T
CLNSRC
CLNACC