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rs9281300

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs9281300(-;-)
Make rs9281300(-;A)
Make rs9281300(A;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271393
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9281300
ebirs9281300
HLIrs9281300
Exacrs9281300
Varsomers9281300
Maprs9281300
PheGenIrs9281300
hapmaprs9281300
1000 genomesrs9281300
hgdprs9281300
ensemblrs9281300
gopubmedrs9281300
geneviewrs9281300
scholarrs9281300
googlers9281300
pharmgkbrs9281300
gwascentralrs9281300
openSNPrs9281300
23andMers9281300
23andMe allrs9281300
SNP Nexus

SNPshotrs9281300
SNPdbers9281300
MSV3drs9281300
GWAS Ctlgrs9281300
GMAF0.4096
Max Magnitude0
ClinVar
Risk rs9281300(A;A)
Alt rs9281300(A;A)
Reference rs9281300(;)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239170_31239171insA
CLNSRC
CLNACC