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rs281860429

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860429(A;G)
Make rs281860429(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271610
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860429
ebirs281860429
HLIrs281860429
Exacrs281860429
Varsomers281860429
Maprs281860429
PheGenIrs281860429
hapmaprs281860429
1000 genomesrs281860429
hgdprs281860429
ensemblrs281860429
gopubmedrs281860429
geneviewrs281860429
scholarrs281860429
googlers281860429
pharmgkbrs281860429
gwascentralrs281860429
openSNPrs281860429
23andMers281860429
23andMe allrs281860429
SNP Nexus

SNPshotrs281860429
SNPdbers281860429
MSV3drs281860429
GWAS Ctlgrs281860429
Max Magnitude0
ClinVar
Risk rs281860429(G;G)
Alt rs281860429(G;G)
Reference rs281860429(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239387T>C
CLNSRC
CLNACC