rs387906524

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs387906524(A;A)

Make rs387906524(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

34377572

Gene

GPI

is a	snp
is	mentioned by
dbSNP	rs387906524
dbSNP (classic)	rs387906524
ClinGen	rs387906524
ebi	rs387906524
HLI	rs387906524
Exac	rs387906524
Gnomad	rs387906524
Varsome	rs387906524
LitVar	rs387906524
Map	rs387906524
PheGenI	rs387906524
Biobank	rs387906524
1000 genomes	rs387906524
hgdp	rs387906524
ensembl	rs387906524
geneview	rs387906524
scholar	rs387906524
google	rs387906524
pharmgkb	rs387906524
gwascentral	rs387906524
openSNP	rs387906524
23andMe	rs387906524
SNPshot	rs387906524
SNPdbe	rs387906524
MSV3d	rs387906524
GWAS Ctlg	rs387906524

Max Magnitude

0

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,