rs587777400

Orientation

plus

Stabilized

minus

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

Make rs587777400(A;A)

Make rs587777400(A;G)

Reference

GRCh38 38.1/142

Chromosome

X

Position

15331653

Gene

PIGA

is a	snp
is	mentioned by
dbSNP	rs587777400
dbSNP (classic)	rs587777400
ClinGen	rs587777400
ebi	rs587777400
HLI	rs587777400
Exac	rs587777400
Gnomad	rs587777400
Varsome	rs587777400
LitVar	rs587777400
Map	rs587777400
PheGenI	rs587777400
Biobank	rs587777400
1000 genomes	rs587777400
hgdp	rs587777400
ensembl	rs587777400
geneview	rs587777400
scholar	rs587777400
google	rs587777400
pharmgkb	rs587777400
gwascentral	rs587777400
openSNP	rs587777400
23andMe	rs587777400
SNPshot	rs587777400
SNPdbe	rs587777400
MSV3d	rs587777400
GWAS Ctlg	rs587777400

Max Magnitude

0

ClinVar
Risk	rs587777400(A;A) Rs587777400(G;G)
Alt	rs587777400(A;A) Rs587777400(G;G)
Reference	Rs587777400(C;C)
Significance	Pathogenic
Disease	Multiple congenital anomalies-hypotonia-seizures syndrome 2
Variation	info
Gene	PIGA
CLNDBN	Multiple congenital anomalies-hypotonia-seizures syndrome 2
Reversed	1
HGVS	NC_000023.10:g.15349775G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000119288.2,