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rs281860434

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860434(C;C)
Make rs281860434(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271603
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860434
ebirs281860434
HLIrs281860434
Exacrs281860434
Varsomers281860434
Maprs281860434
PheGenIrs281860434
hapmaprs281860434
1000 genomesrs281860434
hgdprs281860434
ensemblrs281860434
gopubmedrs281860434
geneviewrs281860434
scholarrs281860434
googlers281860434
pharmgkbrs281860434
gwascentralrs281860434
openSNPrs281860434
23andMers281860434
23andMe allrs281860434
SNP Nexus

SNPshotrs281860434
SNPdbers281860434
MSV3drs281860434
GWAS Ctlgrs281860434
Max Magnitude0
ClinVar
Risk rs281860434(C;C)
Alt rs281860434(C;C)
Reference rs281860434(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239380C>G
CLNSRC
CLNACC