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rs281860499

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860499(-;-)
Make rs281860499(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271193
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860499
ebirs281860499
HLIrs281860499
Exacrs281860499
Varsomers281860499
Maprs281860499
PheGenIrs281860499
hapmaprs281860499
1000 genomesrs281860499
hgdprs281860499
ensemblrs281860499
gopubmedrs281860499
geneviewrs281860499
scholarrs281860499
googlers281860499
pharmgkbrs281860499
gwascentralrs281860499
openSNPrs281860499
23andMers281860499
23andMe allrs281860499
SNP Nexus

SNPshotrs281860499
SNPdbers281860499
MSV3drs281860499
GWAS Ctlgrs281860499
Max Magnitude0
ClinVar
Risk rs281860499(;)
Alt rs281860499(;)
Reference rs281860499(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238970delT
CLNSRC
CLNACC