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rs281860567

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860567(A;A)
Make rs281860567(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270331
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860567
ebirs281860567
HLIrs281860567
Exacrs281860567
Varsomers281860567
Maprs281860567
PheGenIrs281860567
hapmaprs281860567
1000 genomesrs281860567
hgdprs281860567
ensemblrs281860567
gopubmedrs281860567
geneviewrs281860567
scholarrs281860567
googlers281860567
pharmgkbrs281860567
gwascentralrs281860567
openSNPrs281860567
23andMers281860567
23andMe allrs281860567
SNP Nexus

SNPshotrs281860567
SNPdbers281860567
MSV3drs281860567
GWAS Ctlgrs281860567
Max Magnitude0
ClinVar
Risk rs281860567(A;A)
Alt rs281860567(A;A)
Reference rs281860567(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238108C>T
CLNSRC
CLNACC