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rs587776728

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(CTT;CTT) 0 common in clinvar
Make rs587776728(-;-)
Make rs587776728(-;AG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position15321637
GenePIGA
is asnp
is mentioned by
dbSNPrs587776728
ebirs587776728
HLIrs587776728
Exacrs587776728
Varsomers587776728
Maprs587776728
PheGenIrs587776728
hapmaprs587776728
1000 genomesrs587776728
hgdprs587776728
ensemblrs587776728
gopubmedrs587776728
geneviewrs587776728
scholarrs587776728
googlers587776728
pharmgkbrs587776728
gwascentralrs587776728
openSNPrs587776728
23andMers587776728
23andMe allrs587776728
SNP Nexus

SNPshotrs587776728
SNPdbers587776728
MSV3drs587776728
GWAS Ctlgrs587776728
Max Magnitude0
ClinVar
Risk rs587776728(AGT,T;AGT,T)
Alt rs587776728(AGT,T;AGT,T)
Reference rs587776728(CTT;CTT)
Significance Pathogenic
Disease Paroxysmal nocturnal hemoglobinuria 1
Variation info
Gene PIGA
CLNDBN Paroxysmal nocturnal hemoglobinuria 1
Reversed 1
HGVS NC_000023.10:g.15339759_15339760delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000010642.4,