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rs137853584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853584(C;C)
Make rs137853584(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position34399933
GeneGPI
is asnp
is mentioned by
dbSNPrs137853584
ebirs137853584
HLIrs137853584
Exacrs137853584
Varsomers137853584
Maprs137853584
PheGenIrs137853584
hapmaprs137853584
1000 genomesrs137853584
hgdprs137853584
ensemblrs137853584
gopubmedrs137853584
geneviewrs137853584
scholarrs137853584
googlers137853584
pharmgkbrs137853584
gwascentralrs137853584
openSNPrs137853584
23andMers137853584
23andMe allrs137853584
SNP Nexus

SNPshotrs137853584
SNPdbers137853584
MSV3drs137853584
GWAS Ctlgrs137853584
Max Magnitude0
OMIM172400
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853584(C,G;C,G)
Alt rs137853584(C,G;C,G)
Reference rs137853584(T;T)
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.34890838T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014611.25,