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rs281860507

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860507(C;C)
Make rs281860507(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271181
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860507
ebirs281860507
HLIrs281860507
Exacrs281860507
Varsomers281860507
Maprs281860507
PheGenIrs281860507
hapmaprs281860507
1000 genomesrs281860507
hgdprs281860507
ensemblrs281860507
gopubmedrs281860507
geneviewrs281860507
scholarrs281860507
googlers281860507
pharmgkbrs281860507
gwascentralrs281860507
openSNPrs281860507
23andMers281860507
23andMe allrs281860507
SNP Nexus

SNPshotrs281860507
SNPdbers281860507
MSV3drs281860507
GWAS Ctlgrs281860507
Max Magnitude0
ClinVar
Risk rs281860507(C;C)
Alt rs281860507(C;C)
Reference rs281860507(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238958A>G
CLNSRC
CLNACC