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rs281860415

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860415(C;T)
Make rs281860415(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271635
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860415
ebirs281860415
HLIrs281860415
Exacrs281860415
Varsomers281860415
Maprs281860415
PheGenIrs281860415
hapmaprs281860415
1000 genomesrs281860415
hgdprs281860415
ensemblrs281860415
gopubmedrs281860415
geneviewrs281860415
scholarrs281860415
googlers281860415
pharmgkbrs281860415
gwascentralrs281860415
openSNPrs281860415
23andMers281860415
23andMe allrs281860415
SNP Nexus

SNPshotrs281860415
SNPdbers281860415
MSV3drs281860415
GWAS Ctlgrs281860415
Max Magnitude0
ClinVar
Risk rs281860415(T;T)
Alt rs281860415(T;T)
Reference rs281860415(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239412G>A
CLNSRC
CLNACC