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

rs281860511

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860511(A;A)
Make rs281860511(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271172
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860511
ebirs281860511
HLIrs281860511
Exacrs281860511
Varsomers281860511
Maprs281860511
PheGenIrs281860511
hapmaprs281860511
1000 genomesrs281860511
hgdprs281860511
ensemblrs281860511
gopubmedrs281860511
geneviewrs281860511
scholarrs281860511
googlers281860511
pharmgkbrs281860511
gwascentralrs281860511
openSNPrs281860511
23andMers281860511
23andMe allrs281860511
SNP Nexus

SNPshotrs281860511
SNPdbers281860511
MSV3drs281860511
GWAS Ctlgrs281860511
Max Magnitude0
ClinVar
Risk rs281860511(A,C;A,C)
Alt rs281860511(A,C;A,C)
Reference rs281860511(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238949C>G; NC_000006.11:g.31238949C>T
CLNSRC
CLNACC