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rs9260192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9260192(A;A)
Make rs9260192(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944628
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260192
dbSNP (classic)rs9260192
ClinGenrs9260192
ebirs9260192
HLIrs9260192
Exacrs9260192
Gnomadrs9260192
Varsomers9260192
LitVarrs9260192
Maprs9260192
PheGenIrs9260192
Biobankrs9260192
1000 genomesrs9260192
hgdprs9260192
ensemblrs9260192
geneviewrs9260192
scholarrs9260192
googlers9260192
pharmgkbrs9260192
gwascentralrs9260192
openSNPrs9260192
23andMers9260192
SNPshotrs9260192
SNPdbers9260192
MSV3drs9260192
GWAS Ctlgrs9260192
Max Magnitude0
ClinVar
Risk rs9260192(A;A) rs9260192(C;C) rs9260192(T;T)
Alt rs9260192(A;A) rs9260192(C;C) rs9260192(T;T)
Reference Rs9260192(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912405G>A
CLNSRC
CLNACC