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rs281860510

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860510(A;A)
Make rs281860510(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271173
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860510
ebirs281860510
HLIrs281860510
Exacrs281860510
Varsomers281860510
Maprs281860510
PheGenIrs281860510
hapmaprs281860510
1000 genomesrs281860510
hgdprs281860510
ensemblrs281860510
gopubmedrs281860510
geneviewrs281860510
scholarrs281860510
googlers281860510
pharmgkbrs281860510
gwascentralrs281860510
openSNPrs281860510
23andMers281860510
23andMe allrs281860510
SNP Nexus

SNPshotrs281860510
SNPdbers281860510
MSV3drs281860510
GWAS Ctlgrs281860510
Max Magnitude0
ClinVar
Risk rs281860510(A;A)
Alt rs281860510(A;A)
Reference rs281860510(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238950C>T
CLNSRC
CLNACC