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rs267606851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606851(A;G)
Make rs267606851(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position34394032
GeneGPI
is asnp
is mentioned by
dbSNPrs267606851
ebirs267606851
HLIrs267606851
Exacrs267606851
Varsomers267606851
Maprs267606851
PheGenIrs267606851
hapmaprs267606851
1000 genomesrs267606851
hgdprs267606851
ensemblrs267606851
gopubmedrs267606851
geneviewrs267606851
scholarrs267606851
googlers267606851
pharmgkbrs267606851
gwascentralrs267606851
openSNPrs267606851
23andMers267606851
23andMe allrs267606851
SNP Nexus

SNPshotrs267606851
SNPdbers267606851
MSV3drs267606851
GWAS Ctlgrs267606851
Max Magnitude0
ClinVar
Risk rs267606851(G;G)
Alt rs267606851(G;G)
Reference rs267606851(A;A)
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.34884937A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014616.25,