Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606852(C;T)
Make rs267606852(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position34365280
GeneGPI
is asnp
is mentioned by
dbSNPrs267606852
ebirs267606852
HLIrs267606852
Exacrs267606852
Varsomers267606852
Maprs267606852
PheGenIrs267606852
hapmaprs267606852
1000 genomesrs267606852
hgdprs267606852
ensemblrs267606852
gopubmedrs267606852
geneviewrs267606852
scholarrs267606852
googlers267606852
pharmgkbrs267606852
gwascentralrs267606852
openSNPrs267606852
23andMers267606852
23andMe allrs267606852
SNP Nexus

SNPshotrs267606852
SNPdbers267606852
MSV3drs267606852
GWAS Ctlgrs267606852
Max Magnitude0
ClinVar
Risk rs267606852(T;T)
Alt rs267606852(T;T)
Reference rs267606852(C;C)
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.34856185C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014617.19,