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rs281860508

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860508(A;A)
Make rs281860508(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271179
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860508
ebirs281860508
HLIrs281860508
Exacrs281860508
Varsomers281860508
Maprs281860508
PheGenIrs281860508
hapmaprs281860508
1000 genomesrs281860508
hgdprs281860508
ensemblrs281860508
gopubmedrs281860508
geneviewrs281860508
scholarrs281860508
googlers281860508
pharmgkbrs281860508
gwascentralrs281860508
openSNPrs281860508
23andMers281860508
23andMe allrs281860508
SNP Nexus

SNPshotrs281860508
SNPdbers281860508
MSV3drs281860508
GWAS Ctlgrs281860508
Max Magnitude0
ClinVar
Risk rs281860508(A,T;A,T)
Alt rs281860508(A,T;A,T)
Reference rs281860508(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238956C>A; NC_000006.11:g.31238956C>T
CLNSRC
CLNACC