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rs281860413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860413(C;T)
Make rs281860413(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271638
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860413
ebirs281860413
HLIrs281860413
Exacrs281860413
Varsomers281860413
Maprs281860413
PheGenIrs281860413
hapmaprs281860413
1000 genomesrs281860413
hgdprs281860413
ensemblrs281860413
gopubmedrs281860413
geneviewrs281860413
scholarrs281860413
googlers281860413
pharmgkbrs281860413
gwascentralrs281860413
openSNPrs281860413
23andMers281860413
23andMe allrs281860413
SNP Nexus

SNPshotrs281860413
SNPdbers281860413
MSV3drs281860413
GWAS Ctlgrs281860413
Max Magnitude0
ClinVar
Risk rs281860413(T;T)
Alt rs281860413(T;T)
Reference rs281860413(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239415G>A
CLNSRC
CLNACC