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rs281860497

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860497(A;A)
Make rs281860497(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271199
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860497
ebirs281860497
HLIrs281860497
Exacrs281860497
Varsomers281860497
Maprs281860497
PheGenIrs281860497
hapmaprs281860497
1000 genomesrs281860497
hgdprs281860497
ensemblrs281860497
gopubmedrs281860497
geneviewrs281860497
scholarrs281860497
googlers281860497
pharmgkbrs281860497
gwascentralrs281860497
openSNPrs281860497
23andMers281860497
23andMe allrs281860497
SNP Nexus

SNPshotrs281860497
SNPdbers281860497
MSV3drs281860497
GWAS Ctlgrs281860497
Max Magnitude0
ClinVar
Risk rs281860497(A,T;A,T)
Alt rs281860497(A,T;A,T)
Reference rs281860497(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238976G>A; NC_000006.11:g.31238976G>T
CLNSRC
CLNACC