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rs281860447

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860447(C;C)
Make rs281860447(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271327
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860447
ebirs281860447
HLIrs281860447
Exacrs281860447
Varsomers281860447
Maprs281860447
PheGenIrs281860447
hapmaprs281860447
1000 genomesrs281860447
hgdprs281860447
ensemblrs281860447
gopubmedrs281860447
geneviewrs281860447
scholarrs281860447
googlers281860447
pharmgkbrs281860447
gwascentralrs281860447
openSNPrs281860447
23andMers281860447
23andMe allrs281860447
SNP Nexus

SNPshotrs281860447
SNPdbers281860447
MSV3drs281860447
GWAS Ctlgrs281860447
Max Magnitude0
ClinVar
Risk rs281860447(C,G;C,G)
Alt rs281860447(C,G;C,G)
Reference rs281860447(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239104A>C; NC_000006.11:g.31239104A>G
CLNSRC
CLNACC