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rs9260127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9260127(C;C)
Make rs9260127(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942701
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260127
ebirs9260127
HLIrs9260127
Exacrs9260127
Varsomers9260127
Maprs9260127
PheGenIrs9260127
hapmaprs9260127
1000 genomesrs9260127
hgdprs9260127
ensemblrs9260127
gopubmedrs9260127
geneviewrs9260127
scholarrs9260127
googlers9260127
pharmgkbrs9260127
gwascentralrs9260127
openSNPrs9260127
23andMers9260127
23andMe allrs9260127
SNP Nexus

SNPshotrs9260127
SNPdbers9260127
MSV3drs9260127
GWAS Ctlgrs9260127
GMAF0.4233
Max Magnitude0
ClinVar
Risk rs9260127(C;C)
Alt rs9260127(C;C)
Reference rs9260127(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910478G>C
CLNSRC
CLNACC