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rs281860432

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860432(C;G)
Make rs281860432(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271606
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860432
ebirs281860432
HLIrs281860432
Exacrs281860432
Varsomers281860432
Maprs281860432
PheGenIrs281860432
hapmaprs281860432
1000 genomesrs281860432
hgdprs281860432
ensemblrs281860432
gopubmedrs281860432
geneviewrs281860432
scholarrs281860432
googlers281860432
pharmgkbrs281860432
gwascentralrs281860432
openSNPrs281860432
23andMers281860432
23andMe allrs281860432
SNP Nexus

SNPshotrs281860432
SNPdbers281860432
MSV3drs281860432
GWAS Ctlgrs281860432
Max Magnitude0
ClinVar
Risk rs281860432(G,T;G,T)
Alt rs281860432(G,T;G,T)
Reference rs281860432(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239383G>A; NC_000006.11:g.31239383G>C
CLNSRC
CLNACC