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rs281860547

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860547(A;A)
Make rs281860547(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271078
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860547
ebirs281860547
HLIrs281860547
Exacrs281860547
Varsomers281860547
Maprs281860547
PheGenIrs281860547
hapmaprs281860547
1000 genomesrs281860547
hgdprs281860547
ensemblrs281860547
gopubmedrs281860547
geneviewrs281860547
scholarrs281860547
googlers281860547
pharmgkbrs281860547
gwascentralrs281860547
openSNPrs281860547
23andMers281860547
23andMe allrs281860547
SNP Nexus

SNPshotrs281860547
SNPdbers281860547
MSV3drs281860547
GWAS Ctlgrs281860547
Max Magnitude0
ClinVar
Risk rs281860547(A,C;A,C)
Alt rs281860547(A,C;A,C)
Reference rs281860547(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238855C>G; NC_000006.11:g.31238855C>T
CLNSRC
CLNACC