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rs398123552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123552(A;G)
Make rs398123552(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154546058
GeneG6PD, IKBKG
is asnp
is mentioned by
dbSNPrs398123552
ebirs398123552
HLIrs398123552
Exacrs398123552
Varsomers398123552
Maprs398123552
PheGenIrs398123552
hapmaprs398123552
1000 genomesrs398123552
hgdprs398123552
ensemblrs398123552
gopubmedrs398123552
geneviewrs398123552
scholarrs398123552
googlers398123552
pharmgkbrs398123552
gwascentralrs398123552
openSNPrs398123552
23andMers398123552
23andMe allrs398123552
SNP Nexus

SNPshotrs398123552
SNPdbers398123552
MSV3drs398123552
GWAS Ctlgrs398123552
Max Magnitude0
ClinVar
Risk rs398123552(G;G)
Alt rs398123552(G;G)
Reference rs398123552(A;A)
Significance Pathogenic
Disease not provided Anemia
Variation info
Gene IKBKG G6PD
CLNDBN not provided Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 0
HGVS NC_000023.10:g.153774273A>G
CLNSRC ClinVar Emory University
CLNACC RCV000079416.3, RCV000175655.1,