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rs281860423

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860423(A;A)
Make rs281860423(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271623
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860423
ebirs281860423
HLIrs281860423
Exacrs281860423
Varsomers281860423
Maprs281860423
PheGenIrs281860423
hapmaprs281860423
1000 genomesrs281860423
hgdprs281860423
ensemblrs281860423
gopubmedrs281860423
geneviewrs281860423
scholarrs281860423
googlers281860423
pharmgkbrs281860423
gwascentralrs281860423
openSNPrs281860423
23andMers281860423
23andMe allrs281860423
SNP Nexus

SNPshotrs281860423
SNPdbers281860423
MSV3drs281860423
GWAS Ctlgrs281860423
Max Magnitude0
ClinVar
Risk rs281860423(A,C;A,C)
Alt rs281860423(A,C;A,C)
Reference rs281860423(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239400C>G; NC_000006.11:g.31239400C>T
CLNSRC
CLNACC