Have questions? Visit https://www.reddit.com/r/SNPedia

rs281860573

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860573(C;C)
Make rs281860573(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270211
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860573
ebirs281860573
HLIrs281860573
Exacrs281860573
Varsomers281860573
Maprs281860573
PheGenIrs281860573
hapmaprs281860573
1000 genomesrs281860573
hgdprs281860573
ensemblrs281860573
gopubmedrs281860573
geneviewrs281860573
scholarrs281860573
googlers281860573
pharmgkbrs281860573
gwascentralrs281860573
openSNPrs281860573
23andMers281860573
23andMe allrs281860573
SNP Nexus

SNPshotrs281860573
SNPdbers281860573
MSV3drs281860573
GWAS Ctlgrs281860573
Max Magnitude0
ClinVar
Risk rs281860573(C;C)
Alt rs281860573(C;C)
Reference rs281860573(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237988C>G
CLNSRC
CLNACC