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rs267606853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606853(C;G)
Make rs267606853(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position34396362
GeneGPI
is asnp
is mentioned by
dbSNPrs267606853
ebirs267606853
HLIrs267606853
Exacrs267606853
Varsomers267606853
Maprs267606853
PheGenIrs267606853
hapmaprs267606853
1000 genomesrs267606853
hgdprs267606853
ensemblrs267606853
gopubmedrs267606853
geneviewrs267606853
scholarrs267606853
googlers267606853
pharmgkbrs267606853
gwascentralrs267606853
openSNPrs267606853
23andMers267606853
23andMe allrs267606853
SNP Nexus

SNPshotrs267606853
SNPdbers267606853
MSV3drs267606853
GWAS Ctlgrs267606853
Max Magnitude0
ClinVar
Risk rs267606853(G;G)
Alt rs267606853(G;G)
Reference rs267606853(C;C)
Significance Pathogenic
Disease Hemolytic anemia
Variation info
Gene GPI
CLNDBN Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
Reversed 0
HGVS NC_000019.9:g.34887267C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014618.25,