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rs281860524

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCACGTGCG;GCACGTGCG) 0 common in clinvar
Make rs281860524(-;-)
Make rs281860524(-;GGCACGTGC)
Make rs281860524(GGCACGTGC;GGCACGTGC)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271128
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860524
ebirs281860524
HLIrs281860524
Exacrs281860524
Varsomers281860524
Maprs281860524
PheGenIrs281860524
hapmaprs281860524
1000 genomesrs281860524
hgdprs281860524
ensemblrs281860524
gopubmedrs281860524
geneviewrs281860524
scholarrs281860524
googlers281860524
pharmgkbrs281860524
gwascentralrs281860524
openSNPrs281860524
23andMers281860524
23andMe allrs281860524
SNP Nexus

SNPshotrs281860524
SNPdbers281860524
MSV3drs281860524
GWAS Ctlgrs281860524
Max Magnitude0
ClinVar
Risk rs281860524(;)
Alt rs281860524(;)
Reference rs281860524(GCACGTGCG;GCACGTGCG)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238905_31238913delGCACGTGCC
CLNSRC
CLNACC