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rs281860498

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860498(G;T)
Make rs281860498(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271197
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860498
ebirs281860498
HLIrs281860498
Exacrs281860498
Varsomers281860498
Maprs281860498
PheGenIrs281860498
hapmaprs281860498
1000 genomesrs281860498
hgdprs281860498
ensemblrs281860498
gopubmedrs281860498
geneviewrs281860498
scholarrs281860498
googlers281860498
pharmgkbrs281860498
gwascentralrs281860498
openSNPrs281860498
23andMers281860498
23andMe allrs281860498
SNP Nexus

SNPshotrs281860498
SNPdbers281860498
MSV3drs281860498
GWAS Ctlgrs281860498
Max Magnitude0
ClinVar
Risk rs281860498(T;T)
Alt rs281860498(T;T)
Reference rs281860498(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238974C>A
CLNSRC
CLNACC