rs587777396

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs587777396(A;A)

Make rs587777396(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

15331576

Gene

PIGA

is a	snp
is	mentioned by
dbSNP	rs587777396
dbSNP (classic)	rs587777396
ClinGen	rs587777396
ebi	rs587777396
HLI	rs587777396
Exac	rs587777396
Gnomad	rs587777396
Varsome	rs587777396
LitVar	rs587777396
Map	rs587777396
PheGenI	rs587777396
Biobank	rs587777396
1000 genomes	rs587777396
hgdp	rs587777396
ensembl	rs587777396
geneview	rs587777396
scholar	rs587777396
google	rs587777396
pharmgkb	rs587777396
gwascentral	rs587777396
openSNP	rs587777396
23andMe	rs587777396
SNPshot	rs587777396
SNPdbe	rs587777396
MSV3d	rs587777396
GWAS Ctlg	rs587777396

Max Magnitude

0

ClinVar
Risk	rs587777396(A;A)
Alt	rs587777396(A;A)
Reference	Rs587777396(G;G)
Significance	Pathogenic
Disease	Multiple congenital anomalies-hypotonia-seizures syndrome 2 not provided
Variation	info
Gene	PIGA
CLNDBN	Multiple congenital anomalies-hypotonia-seizures syndrome 2 not provided
Reversed	0
HGVS	NC_000023.10:g.15349698G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000119283.2, RCV000443275.1,