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rs281860501

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860501(C;T)
Make rs281860501(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271192
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860501
ebirs281860501
HLIrs281860501
Exacrs281860501
Varsomers281860501
Maprs281860501
PheGenIrs281860501
hapmaprs281860501
1000 genomesrs281860501
hgdprs281860501
ensemblrs281860501
gopubmedrs281860501
geneviewrs281860501
scholarrs281860501
googlers281860501
pharmgkbrs281860501
gwascentralrs281860501
openSNPrs281860501
23andMers281860501
23andMe allrs281860501
SNP Nexus

SNPshotrs281860501
SNPdbers281860501
MSV3drs281860501
GWAS Ctlgrs281860501
Max Magnitude0
ClinVar
Risk rs281860501(T;T)
Alt rs281860501(T;T)
Reference rs281860501(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238969G>A
CLNSRC
CLNACC