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rs281860525

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860525(A;A)
Make rs281860525(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271135
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860525
ebirs281860525
HLIrs281860525
Exacrs281860525
Varsomers281860525
Maprs281860525
PheGenIrs281860525
hapmaprs281860525
1000 genomesrs281860525
hgdprs281860525
ensemblrs281860525
gopubmedrs281860525
geneviewrs281860525
scholarrs281860525
googlers281860525
pharmgkbrs281860525
gwascentralrs281860525
openSNPrs281860525
23andMers281860525
23andMe allrs281860525
SNP Nexus

SNPshotrs281860525
SNPdbers281860525
MSV3drs281860525
GWAS Ctlgrs281860525
Max Magnitude0
ClinVar
Risk rs281860525(A;A)
Alt rs281860525(A;A)
Reference rs281860525(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238912C>T
CLNSRC
CLNACC