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rs281860412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860412(A;A)
Make rs281860412(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271639
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860412
dbSNP (old)rs281860412
ClinGenrs281860412
ebirs281860412
HLIrs281860412
Exacrs281860412
Gnomadrs281860412
Varsomers281860412
Maprs281860412
PheGenIrs281860412
Biobankrs281860412
1000 genomesrs281860412
hgdprs281860412
ensemblrs281860412
gopubmedrs281860412
geneviewrs281860412
scholarrs281860412
googlers281860412
pharmgkbrs281860412
gwascentralrs281860412
openSNPrs281860412
23andMers281860412
23andMe allrs281860412
SNP Nexus

SNPshotrs281860412
SNPdbers281860412
MSV3drs281860412
GWAS Ctlgrs281860412
Max Magnitude0
ClinVar
Risk rs281860412(A;A) rs281860412(T;T)
Alt rs281860412(A;A) rs281860412(T;T)
Reference Rs281860412(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239416G>A; NC_000006.11:g.31239416G>T
CLNSRC
CLNACC