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rs281860500

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860500(-;-)
Make rs281860500(-;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271192
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860500
ebirs281860500
HLIrs281860500
Exacrs281860500
Varsomers281860500
Maprs281860500
PheGenIrs281860500
hapmaprs281860500
1000 genomesrs281860500
hgdprs281860500
ensemblrs281860500
gopubmedrs281860500
geneviewrs281860500
scholarrs281860500
googlers281860500
pharmgkbrs281860500
gwascentralrs281860500
openSNPrs281860500
23andMers281860500
23andMe allrs281860500
SNP Nexus

SNPshotrs281860500
SNPdbers281860500
MSV3drs281860500
GWAS Ctlgrs281860500
Max Magnitude0
ClinVar
Risk rs281860500(;)
Alt rs281860500(;)
Reference rs281860500(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238969delG
CLNSRC
CLNACC