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rs281860577

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860577(-;-)
Make rs281860577(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270121
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860577
ebirs281860577
HLIrs281860577
Exacrs281860577
Varsomers281860577
Maprs281860577
PheGenIrs281860577
hapmaprs281860577
1000 genomesrs281860577
hgdprs281860577
ensemblrs281860577
gopubmedrs281860577
geneviewrs281860577
scholarrs281860577
googlers281860577
pharmgkbrs281860577
gwascentralrs281860577
openSNPrs281860577
23andMers281860577
23andMe allrs281860577
SNP Nexus

SNPshotrs281860577
SNPdbers281860577
MSV3drs281860577
GWAS Ctlgrs281860577
Max Magnitude0
ClinVar
Risk rs281860577(;)
Alt rs281860577(;)
Reference rs281860577(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237898delC
CLNSRC
CLNACC