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rs281860513

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860513(C;T)
Make rs281860513(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271162
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860513
ClinGenrs281860513
ebirs281860513
HLIrs281860513
Exacrs281860513
Varsomers281860513
Maprs281860513
PheGenIrs281860513
hapmaprs281860513
1000 genomesrs281860513
hgdprs281860513
ensemblrs281860513
gopubmedrs281860513
geneviewrs281860513
scholarrs281860513
googlers281860513
pharmgkbrs281860513
gwascentralrs281860513
openSNPrs281860513
23andMers281860513
23andMe allrs281860513
SNP Nexus

SNPshotrs281860513
SNPdbers281860513
MSV3drs281860513
GWAS Ctlgrs281860513
Max Magnitude0
ClinVar
Risk rs281860513(T;T)
Alt rs281860513(T;T)
Reference Rs281860513(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238939G>A
CLNSRC
CLNACC