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rs137853582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853582(A;A)
Make rs137853582(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position34377575
GeneGPI
is asnp
is mentioned by
dbSNPrs137853582
ebirs137853582
HLIrs137853582
Exacrs137853582
Varsomers137853582
Maprs137853582
PheGenIrs137853582
hapmaprs137853582
1000 genomesrs137853582
hgdprs137853582
ensemblrs137853582
gopubmedrs137853582
geneviewrs137853582
scholarrs137853582
googlers137853582
pharmgkbrs137853582
gwascentralrs137853582
openSNPrs137853582
23andMers137853582
23andMe allrs137853582
SNP Nexus

SNPshotrs137853582
SNPdbers137853582
MSV3drs137853582
GWAS Ctlgrs137853582
Max Magnitude0
OMIM172400
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853582(A;A)
Alt rs137853582(A;A)
Reference rs137853582(G;G)
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.34868480G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014609.24,