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rs281860426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860426(A;G)
Make rs281860426(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271614
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860426
ebirs281860426
HLIrs281860426
Exacrs281860426
Varsomers281860426
Maprs281860426
PheGenIrs281860426
hapmaprs281860426
1000 genomesrs281860426
hgdprs281860426
ensemblrs281860426
gopubmedrs281860426
geneviewrs281860426
scholarrs281860426
googlers281860426
pharmgkbrs281860426
gwascentralrs281860426
openSNPrs281860426
23andMers281860426
23andMe allrs281860426
SNP Nexus

SNPshotrs281860426
SNPdbers281860426
MSV3drs281860426
GWAS Ctlgrs281860426
Max Magnitude0
ClinVar
Risk rs281860426(G;G)
Alt rs281860426(G;G)
Reference rs281860426(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239391T>C
CLNSRC
CLNACC