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rs281860488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860488(A;A)
Make rs281860488(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271231
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860488
ebirs281860488
HLIrs281860488
Exacrs281860488
Varsomers281860488
Maprs281860488
PheGenIrs281860488
hapmaprs281860488
1000 genomesrs281860488
hgdprs281860488
ensemblrs281860488
gopubmedrs281860488
geneviewrs281860488
scholarrs281860488
googlers281860488
pharmgkbrs281860488
gwascentralrs281860488
openSNPrs281860488
23andMers281860488
23andMe allrs281860488
SNP Nexus

SNPshotrs281860488
SNPdbers281860488
MSV3drs281860488
GWAS Ctlgrs281860488
Max Magnitude0
ClinVar
Risk rs281860488(A,C;A,C)
Alt rs281860488(A,C;A,C)
Reference rs281860488(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239008A>G; NC_000006.11:g.31239008A>T
CLNSRC
CLNACC