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rs137853585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853585(A;A)
Make rs137853585(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position34399974
GeneGPI
is asnp
is mentioned by
dbSNPrs137853585
ebirs137853585
HLIrs137853585
Exacrs137853585
Varsomers137853585
Maprs137853585
PheGenIrs137853585
hapmaprs137853585
1000 genomesrs137853585
hgdprs137853585
ensemblrs137853585
gopubmedrs137853585
geneviewrs137853585
scholarrs137853585
googlers137853585
pharmgkbrs137853585
gwascentralrs137853585
openSNPrs137853585
23andMers137853585
23andMe allrs137853585
SNP Nexus

SNPshotrs137853585
SNPdbers137853585
MSV3drs137853585
GWAS Ctlgrs137853585
Max Magnitude0
OMIM172400
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853585(A;A)
Alt rs137853585(A;A)
Reference rs137853585(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.34890879G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014612.26,