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rs587776726

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776726(-;-)
Make rs587776726(-;AC)
Make rs587776726(AC;AC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position15331681
GenePIGA
is asnp
is mentioned by
dbSNPrs587776726
ebirs587776726
HLIrs587776726
Exacrs587776726
Varsomers587776726
Maprs587776726
PheGenIrs587776726
hapmaprs587776726
1000 genomesrs587776726
hgdprs587776726
ensemblrs587776726
gopubmedrs587776726
geneviewrs587776726
scholarrs587776726
googlers587776726
pharmgkbrs587776726
gwascentralrs587776726
openSNPrs587776726
23andMers587776726
23andMe allrs587776726
SNP Nexus

SNPshotrs587776726
SNPdbers587776726
MSV3drs587776726
GWAS Ctlgrs587776726
Max Magnitude0
ClinVar
Risk rs587776726(AC;AC)
Alt rs587776726(AC;AC)
Reference rs587776726(;)
Significance Pathogenic
Disease Paroxysmal nocturnal hemoglobinuria 1
Variation info
Gene PIGA
CLNDBN Paroxysmal nocturnal hemoglobinuria 1
Reversed 1
HGVS NC_000023.10:g.15349803_15349804insAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010640.2,