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

rs587776725

From SNPedia

Orientationplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776725(-;-)
Make rs587776725(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position15324738
GenePIGA
is asnp
is mentioned by
dbSNPrs587776725
ebirs587776725
HLIrs587776725
Exacrs587776725
Varsomers587776725
Maprs587776725
PheGenIrs587776725
hapmaprs587776725
1000 genomesrs587776725
hgdprs587776725
ensemblrs587776725
gopubmedrs587776725
geneviewrs587776725
scholarrs587776725
googlers587776725
pharmgkbrs587776725
gwascentralrs587776725
openSNPrs587776725
23andMers587776725
23andMe allrs587776725
SNP Nexus

SNPshotrs587776725
SNPdbers587776725
MSV3drs587776725
GWAS Ctlgrs587776725
Max Magnitude0
ClinVar
Risk rs587776725(GA,A;GA,A)
Alt rs587776725(GA,A;GA,A)
Reference rs587776725(CA;CA)
Significance Pathogenic
Disease Paroxysmal nocturnal hemoglobinuria 1
Variation info
Gene PIGA
CLNDBN Paroxysmal nocturnal hemoglobinuria 1
Reversed 1
HGVS NC_000023.10:g.15342860delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000010638.3,