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rs587776724

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587776724(-;T)
Make rs587776724(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position15331471
GenePIGA
is asnp
is mentioned by
dbSNPrs587776724
dbSNP (classic)rs587776724
ClinGenrs587776724
ebirs587776724
HLIrs587776724
Exacrs587776724
Gnomadrs587776724
Varsomers587776724
LitVarrs587776724
Maprs587776724
PheGenIrs587776724
Biobankrs587776724
1000 genomesrs587776724
hgdprs587776724
ensemblrs587776724
geneviewrs587776724
scholarrs587776724
googlers587776724
pharmgkbrs587776724
gwascentralrs587776724
openSNPrs587776724
23andMers587776724
SNPshotrs587776724
SNPdbers587776724
MSV3drs587776724
GWAS Ctlgrs587776724
Max Magnitude0
ClinVar
Risk rs587776724(T;T)
Alt rs587776724(T;T)
Reference Rs587776724(-;-)
Significance Pathogenic
Disease Paroxysmal nocturnal hemoglobinuria 1
Variation info
Gene PIGA
CLNDBN Paroxysmal nocturnal hemoglobinuria 1
Reversed 1
HGVS NC_000023.10:g.15349593_15349594insT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010637.2,