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rs387906524

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906524(A;A)
Make rs387906524(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position34377572
GeneGPI
is asnp
is mentioned by
dbSNPrs387906524
ebirs387906524
HLIrs387906524
Exacrs387906524
Varsomers387906524
Maprs387906524
PheGenIrs387906524
hapmaprs387906524
1000 genomesrs387906524
hgdprs387906524
ensemblrs387906524
gopubmedrs387906524
geneviewrs387906524
scholarrs387906524
googlers387906524
pharmgkbrs387906524
gwascentralrs387906524
openSNPrs387906524
23andMers387906524
23andMe allrs387906524
SNP Nexus

SNPshotrs387906524
SNPdbers387906524
MSV3drs387906524
GWAS Ctlgrs387906524
Max Magnitude0
ClinVar
Risk rs387906524(A;A)
Alt rs387906524(A;A)
Reference rs387906524(G;G)
Significance Pathogenic
Disease Hemolytic anemia
Variation info
Gene
CLNDBN Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
Reversed 0
HGVS NC_000019.9:g.34868477G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014609.1,