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rs281860512

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860512(C;G)
Make rs281860512(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271170
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860512
ebirs281860512
HLIrs281860512
Exacrs281860512
Varsomers281860512
Maprs281860512
PheGenIrs281860512
hapmaprs281860512
1000 genomesrs281860512
hgdprs281860512
ensemblrs281860512
gopubmedrs281860512
geneviewrs281860512
scholarrs281860512
googlers281860512
pharmgkbrs281860512
gwascentralrs281860512
openSNPrs281860512
23andMers281860512
23andMe allrs281860512
SNP Nexus

SNPshotrs281860512
SNPdbers281860512
MSV3drs281860512
GWAS Ctlgrs281860512
Max Magnitude0
ClinVar
Risk rs281860512(G;G)
Alt rs281860512(G;G)
Reference rs281860512(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238947G>C
CLNSRC
CLNACC