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rs281860414

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860414(C;C)
Make rs281860414(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271637
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860414
ebirs281860414
HLIrs281860414
Exacrs281860414
Varsomers281860414
Maprs281860414
PheGenIrs281860414
hapmaprs281860414
1000 genomesrs281860414
hgdprs281860414
ensemblrs281860414
gopubmedrs281860414
geneviewrs281860414
scholarrs281860414
googlers281860414
pharmgkbrs281860414
gwascentralrs281860414
openSNPrs281860414
23andMers281860414
23andMe allrs281860414
SNP Nexus

SNPshotrs281860414
SNPdbers281860414
MSV3drs281860414
GWAS Ctlgrs281860414
Max Magnitude0
ClinVar
Risk rs281860414(C,G;C,G)
Alt rs281860414(C,G;C,G)
Reference rs281860414(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239414A>C; NC_000006.11:g.31239414A>G
CLNSRC
CLNACC