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rs281860515

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860515(A;G)
Make rs281860515(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271156
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860515
ebirs281860515
HLIrs281860515
Exacrs281860515
Varsomers281860515
Maprs281860515
PheGenIrs281860515
hapmaprs281860515
1000 genomesrs281860515
hgdprs281860515
ensemblrs281860515
gopubmedrs281860515
geneviewrs281860515
scholarrs281860515
googlers281860515
pharmgkbrs281860515
gwascentralrs281860515
openSNPrs281860515
23andMers281860515
23andMe allrs281860515
SNP Nexus

SNPshotrs281860515
SNPdbers281860515
MSV3drs281860515
GWAS Ctlgrs281860515
Max Magnitude0
ClinVar
Risk rs281860515(G;G)
Alt rs281860515(G;G)
Reference rs281860515(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238933T>C
CLNSRC
CLNACC