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rs281860550

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860550(C;C)
Make rs281860550(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270468
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860550
ebirs281860550
HLIrs281860550
Exacrs281860550
Varsomers281860550
Maprs281860550
PheGenIrs281860550
hapmaprs281860550
1000 genomesrs281860550
hgdprs281860550
ensemblrs281860550
gopubmedrs281860550
geneviewrs281860550
scholarrs281860550
googlers281860550
pharmgkbrs281860550
gwascentralrs281860550
openSNPrs281860550
23andMers281860550
23andMe allrs281860550
SNP Nexus

SNPshotrs281860550
SNPdbers281860550
MSV3drs281860550
GWAS Ctlgrs281860550
Max Magnitude0
ClinVar
Risk rs281860550(C;C)
Alt rs281860550(C;C)
Reference rs281860550(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238245C>G
CLNSRC
CLNACC