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rs281860555

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860555(-;-)
Make rs281860555(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270428
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860555
ebirs281860555
HLIrs281860555
Exacrs281860555
Varsomers281860555
Maprs281860555
PheGenIrs281860555
hapmaprs281860555
1000 genomesrs281860555
hgdprs281860555
ensemblrs281860555
gopubmedrs281860555
geneviewrs281860555
scholarrs281860555
googlers281860555
pharmgkbrs281860555
gwascentralrs281860555
openSNPrs281860555
23andMers281860555
23andMe allrs281860555
SNP Nexus

SNPshotrs281860555
SNPdbers281860555
MSV3drs281860555
GWAS Ctlgrs281860555
Max Magnitude0
ClinVar
Risk rs281860555(;)
Alt rs281860555(;)
Reference rs281860555(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238205delC
CLNSRC
CLNACC