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rs281860398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860398(A;A)
Make rs281860398(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271677
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860398
ebirs281860398
HLIrs281860398
Exacrs281860398
Varsomers281860398
Maprs281860398
PheGenIrs281860398
hapmaprs281860398
1000 genomesrs281860398
hgdprs281860398
ensemblrs281860398
gopubmedrs281860398
geneviewrs281860398
scholarrs281860398
googlers281860398
pharmgkbrs281860398
gwascentralrs281860398
openSNPrs281860398
23andMers281860398
23andMe allrs281860398
SNP Nexus

SNPshotrs281860398
SNPdbers281860398
MSV3drs281860398
GWAS Ctlgrs281860398
Max Magnitude0
ClinVar
Risk rs281860398(A,G;A,G)
Alt rs281860398(A,G;A,G)
Reference rs281860398(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239454G>C; NC_000006.11:g.31239454G>T
CLNSRC
CLNACC