Have questions? Visit https://www.reddit.com/r/SNPedia

rs2515904

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2515904(C;G)
Make rs2515904(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154534556
GeneG6PD
is asnp
is mentioned by
dbSNPrs2515904
dbSNP (classic)rs2515904
ClinGenrs2515904
ebirs2515904
HLIrs2515904
Exacrs2515904
Gnomadrs2515904
Varsomers2515904
LitVarrs2515904
Maprs2515904
PheGenIrs2515904
Biobankrs2515904
1000 genomesrs2515904
hgdprs2515904
ensemblrs2515904
geneviewrs2515904
scholarrs2515904
googlers2515904
pharmgkbrs2515904
gwascentralrs2515904
openSNPrs2515904
23andMers2515904
23andMe allrs2515904
SNPshotrs2515904
SNPdbers2515904
MSV3drs2515904
GWAS Ctlgrs2515904
Max Magnitude0
? (C;C) (C;G) (G;G) 28


ClinVar
Risk rs2515904(G;G)
Alt rs2515904(G;G)
Reference Rs2515904(C;C)
Significance Pathogenic
Disease Glucose 6 phosphate dehydrogenase deficiency
Variation info
Gene G6PD
CLNDBN Glucose 6 phosphate dehydrogenase deficiency
Reversed 1
HGVS NC_000023.10:g.153762771G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011095.5,