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rs281860514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860514(C;C)
Make rs281860514(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271160
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860514
ebirs281860514
HLIrs281860514
Exacrs281860514
Varsomers281860514
Maprs281860514
PheGenIrs281860514
hapmaprs281860514
1000 genomesrs281860514
hgdprs281860514
ensemblrs281860514
gopubmedrs281860514
geneviewrs281860514
scholarrs281860514
googlers281860514
pharmgkbrs281860514
gwascentralrs281860514
openSNPrs281860514
23andMers281860514
23andMe allrs281860514
SNP Nexus

SNPshotrs281860514
SNPdbers281860514
MSV3drs281860514
GWAS Ctlgrs281860514
Max Magnitude0
ClinVar
Risk rs281860514(C;C)
Alt rs281860514(C;C)
Reference rs281860514(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238937C>G
CLNSRC
CLNACC