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rs150666121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs150666121(A;A)
Make rs150666121(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944961
GeneHLA-A
is asnp
is mentioned by
dbSNPrs150666121
ebirs150666121
HLIrs150666121
Exacrs150666121
Varsomers150666121
Maprs150666121
PheGenIrs150666121
hapmaprs150666121
1000 genomesrs150666121
hgdprs150666121
ensemblrs150666121
gopubmedrs150666121
geneviewrs150666121
scholarrs150666121
googlers150666121
pharmgkbrs150666121
gwascentralrs150666121
openSNPrs150666121
23andMers150666121
23andMe allrs150666121
SNP Nexus

SNPshotrs150666121
SNPdbers150666121
MSV3drs150666121
GWAS Ctlgrs150666121
GMAF0.004591
Max Magnitude0
ClinVar
Risk rs150666121(A;A)
Alt rs150666121(A;A)
Reference rs150666121(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912738T>A
CLNSRC
CLNACC