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rs281860492

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860492(C;C)
Make rs281860492(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271221
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860492
ebirs281860492
HLIrs281860492
Exacrs281860492
Varsomers281860492
Maprs281860492
PheGenIrs281860492
hapmaprs281860492
1000 genomesrs281860492
hgdprs281860492
ensemblrs281860492
gopubmedrs281860492
geneviewrs281860492
scholarrs281860492
googlers281860492
pharmgkbrs281860492
gwascentralrs281860492
openSNPrs281860492
23andMers281860492
23andMe allrs281860492
SNP Nexus

SNPshotrs281860492
SNPdbers281860492
MSV3drs281860492
GWAS Ctlgrs281860492
Max Magnitude0
ClinVar
Risk rs281860492(C;C)
Alt rs281860492(C;C)
Reference rs281860492(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238998C>G
CLNSRC
CLNACC