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rs34193178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs34193178(C;G)
Make rs34193178(G;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position154532945
GeneG6PD
is asnp
is mentioned by
dbSNPrs34193178
ebirs34193178
HLIrs34193178
Exacrs34193178
Varsomers34193178
Maprs34193178
PheGenIrs34193178
hapmaprs34193178
1000 genomesrs34193178
hgdprs34193178
ensemblrs34193178
gopubmedrs34193178
geneviewrs34193178
scholarrs34193178
googlers34193178
pharmgkbrs34193178
gwascentralrs34193178
openSNPrs34193178
23andMers34193178
23andMe allrs34193178
SNP Nexus

SNPshotrs34193178
SNPdbers34193178
MSV3drs34193178
GWAS Ctlgrs34193178
Max Magnitude0
ClinVar
Risk rs34193178(G,T;G,T)
Alt rs34193178(G,T;G,T)
Reference rs34193178(C;C)
Significance Pathogenic
Disease not provided Anemia
Variation info
Gene G6PD
CLNDBN not provided Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 0
HGVS NC_000023.10:g.153761160C>G
CLNSRC HGMD
CLNACC RCV000079391.3, RCV000180548.1,