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rs281860528

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTGGAG;GTGGAG) 0 common in clinvar
Make rs281860528(-;-)
Make rs281860528(-;GTGGAG)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271122
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860528
ebirs281860528
HLIrs281860528
Exacrs281860528
Varsomers281860528
Maprs281860528
PheGenIrs281860528
hapmaprs281860528
1000 genomesrs281860528
hgdprs281860528
ensemblrs281860528
gopubmedrs281860528
geneviewrs281860528
scholarrs281860528
googlers281860528
pharmgkbrs281860528
gwascentralrs281860528
openSNPrs281860528
23andMers281860528
23andMe allrs281860528
SNP Nexus

SNPshotrs281860528
SNPdbers281860528
MSV3drs281860528
GWAS Ctlgrs281860528
Max Magnitude0
ClinVar
Risk rs281860528(;)
Alt rs281860528(;)
Reference rs281860528(GTGGAG;GTGGAG)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238899_31238904delCTCCAC
CLNSRC
CLNACC