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rs9260123

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9260123(C;G)
Make rs9260123(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942652
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260123
dbSNP (classic)rs9260123
ClinGenrs9260123
ebirs9260123
HLIrs9260123
Exacrs9260123
Gnomadrs9260123
Varsomers9260123
LitVarrs9260123
Maprs9260123
PheGenIrs9260123
Biobankrs9260123
1000 genomesrs9260123
hgdprs9260123
ensemblrs9260123
geneviewrs9260123
scholarrs9260123
googlers9260123
pharmgkbrs9260123
gwascentralrs9260123
openSNPrs9260123
23andMers9260123
SNPshotrs9260123
SNPdbers9260123
MSV3drs9260123
GWAS Ctlgrs9260123
GMAF0.4899
Max Magnitude0
ClinVar
Risk rs9260123(G;G)
Alt rs9260123(G;G)
Reference Rs9260123(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910429C>G
CLNSRC
CLNACC