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rs281860540

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860540(C;C)
Make rs281860540(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271105
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860540
ebirs281860540
HLIrs281860540
Exacrs281860540
Varsomers281860540
Maprs281860540
PheGenIrs281860540
hapmaprs281860540
1000 genomesrs281860540
hgdprs281860540
ensemblrs281860540
gopubmedrs281860540
geneviewrs281860540
scholarrs281860540
googlers281860540
pharmgkbrs281860540
gwascentralrs281860540
openSNPrs281860540
23andMers281860540
23andMe allrs281860540
SNP Nexus

SNPshotrs281860540
SNPdbers281860540
MSV3drs281860540
GWAS Ctlgrs281860540
Max Magnitude0
ClinVar
Risk rs281860540(C,G;C,G)
Alt rs281860540(C,G;C,G)
Reference rs281860540(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238882A>C; NC_000006.11:g.31238882A>G
CLNSRC
CLNACC