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rs281860471

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860471(A;G)
Make rs281860471(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271267
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860471
ebirs281860471
HLIrs281860471
Exacrs281860471
Varsomers281860471
Maprs281860471
PheGenIrs281860471
hapmaprs281860471
1000 genomesrs281860471
hgdprs281860471
ensemblrs281860471
gopubmedrs281860471
geneviewrs281860471
scholarrs281860471
googlers281860471
pharmgkbrs281860471
gwascentralrs281860471
openSNPrs281860471
23andMers281860471
23andMe allrs281860471
SNP Nexus

SNPshotrs281860471
SNPdbers281860471
MSV3drs281860471
GWAS Ctlgrs281860471
Max Magnitude0
ClinVar
Risk rs281860471(G;G)
Alt rs281860471(G;G)
Reference rs281860471(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239044T>C
CLNSRC
CLNACC