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rs9260152

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9260152(C;C)
Make rs9260152(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943260
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260152
ebirs9260152
HLIrs9260152
Exacrs9260152
Varsomers9260152
Maprs9260152
PheGenIrs9260152
hapmaprs9260152
1000 genomesrs9260152
hgdprs9260152
ensemblrs9260152
gopubmedrs9260152
geneviewrs9260152
scholarrs9260152
googlers9260152
pharmgkbrs9260152
gwascentralrs9260152
openSNPrs9260152
23andMers9260152
23andMe allrs9260152
SNP Nexus

SNPshotrs9260152
SNPdbers9260152
MSV3drs9260152
GWAS Ctlgrs9260152
GMAF0.3356
Max Magnitude0
ClinVar
Risk rs9260152(C;C)
Alt rs9260152(C;C)
Reference rs9260152(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911037G>C
CLNSRC
CLNACC