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rs281860400

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860400(A;A)
Make rs281860400(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271675
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860400
ebirs281860400
HLIrs281860400
Exacrs281860400
Varsomers281860400
Maprs281860400
PheGenIrs281860400
hapmaprs281860400
1000 genomesrs281860400
hgdprs281860400
ensemblrs281860400
gopubmedrs281860400
geneviewrs281860400
scholarrs281860400
googlers281860400
pharmgkbrs281860400
gwascentralrs281860400
openSNPrs281860400
23andMers281860400
23andMe allrs281860400
SNP Nexus

SNPshotrs281860400
SNPdbers281860400
MSV3drs281860400
GWAS Ctlgrs281860400
Max Magnitude0
ClinVar
Risk rs281860400(A;A)
Alt rs281860400(A;A)
Reference rs281860400(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239452C>T
CLNSRC
CLNACC