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rs281860422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860422(C;T)
Make rs281860422(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271624
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860422
ebirs281860422
HLIrs281860422
Exacrs281860422
Varsomers281860422
Maprs281860422
PheGenIrs281860422
hapmaprs281860422
1000 genomesrs281860422
hgdprs281860422
ensemblrs281860422
gopubmedrs281860422
geneviewrs281860422
scholarrs281860422
googlers281860422
pharmgkbrs281860422
gwascentralrs281860422
openSNPrs281860422
23andMers281860422
23andMe allrs281860422
SNP Nexus

SNPshotrs281860422
SNPdbers281860422
MSV3drs281860422
GWAS Ctlgrs281860422
Max Magnitude0
ClinVar
Risk rs281860422(T;T)
Alt rs281860422(T;T)
Reference rs281860422(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239401G>A
CLNSRC
CLNACC