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rs281860542

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860542(A;A)
Make rs281860542(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271101
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860542
ebirs281860542
HLIrs281860542
Exacrs281860542
Varsomers281860542
Maprs281860542
PheGenIrs281860542
hapmaprs281860542
1000 genomesrs281860542
hgdprs281860542
ensemblrs281860542
gopubmedrs281860542
geneviewrs281860542
scholarrs281860542
googlers281860542
pharmgkbrs281860542
gwascentralrs281860542
openSNPrs281860542
23andMers281860542
23andMe allrs281860542
SNP Nexus

SNPshotrs281860542
SNPdbers281860542
MSV3drs281860542
GWAS Ctlgrs281860542
Max Magnitude0
ClinVar
Risk rs281860542(A;A)
Alt rs281860542(A;A)
Reference rs281860542(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238878C>T
CLNSRC
CLNACC